Canonical Allele Identifier: PA1139743268
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 177878
ClinVar RCV Id: RCV000154526
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361187.1:p.Lys523Asn
CA273507
NM_001374258.1:c.1569A>C
CA369588490
NM_001374258.1:c.1569A>T