Canonical Allele Identifier: PA2828778312
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 2156732
ClinVar RCV Id: RCV003090990 RCV003228116
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365401.1:p.Gly263Arg
CA369590377
NM_001378472.1:c.787G>C
CA369590378
NM_001378472.1:c.787G>A