Canonical Allele Identifier: PA2828779170
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 3223978
ClinVar RCV Id: RCV004516742
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365402.1:p.Ala509Ser
CA369587791
NM_001378473.1:c.1525G>T