Canonical Allele Identifier: PA135087
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 44803
ClinVar RCV Id: RCV000037919 RCV000425868 RCV000436583 RCV000418480 RCV000427987 RCV000420102 RCV000445054 RCV000430773 RCV000435417 RCV000436805
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004324.2:p.Gly469Val
CA135085
NM_004333.6:c.1406G>T