Canonical Allele Identifier: PA2828775939
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 864012
ClinVar RCV Id: RCV001071102
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365397.1:p.Leu541Phe
CA369588073
NM_001378468.1:c.1621C>T