Canonical Allele Identifier: PA2828777197
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13970
ClinVar RCV Id: RCV000015004 RCV000033306 RCV000421772 RCV000422506 RCV000423124 RCV000428425 RCV000428973 RCV000433203 RCV000439657 RCV000439076 RCV000441999 RCV001778653
ClinVar Variation Id: 177775
ClinVar RCV Id: RCV000154398 RCV000433832 RCV001813396
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365399.1:p.Gly435Arg
CA123653
NM_001378470.1:c.1303G>C
CA180746
NM_001378470.1:c.1303G>A