Canonical Allele Identifier: PA2828776759
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 162795
ClinVar RCV Id: RCV000150197 RCV000788373 RCV000824929 RCV001374414 RCV001850036 RCV003224801
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365398.1:p.Ala690Asp
CA273127
NM_001378469.1:c.2069C>A