Canonical Allele Identifier: PA2828776132
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 133719
ClinVar RCV Id: RCV000120255
ClinVar Variation Id: 945335
ClinVar RCV Id: RCV001215954 RCV003433083
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365398.1:p.Gly21Arg
CA157468
NM_001378469.1:c.61G>A
CA369590175
NM_001378469.1:c.61G>C