Canonical Allele Identifier: PA2828474601
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711053
ClinVar RCV Id: RCV002292340
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361173.1:p.Val499Gly
CA369588924
NM_001374244.1:c.1496T>G