Canonical Allele Identifier: PA2828778001
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 376375
ClinVar RCV Id: RCV000425257 RCV000432706 RCV000435960 RCV000442687
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365400.1:p.Gly559Asp
CA16602814
NM_001378471.1:c.1676G>A