Canonical Allele Identifier: PA2828780392
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1905687
ClinVar RCV Id: RCV002583696
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365404.1:p.Ser379Leu
CA168090516
NM_001378475.1:c.1136C>T