Canonical Allele Identifier: PA2828780501
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 44811
ClinVar RCV Id: RCV000037929 RCV000524048 RCV000763165
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365404.1:p.Asn493Lys
CA280022
NM_001378475.1:c.1479T>A
CA369543395
NM_001378475.1:c.1479T>G