Canonical Allele Identifier: PA1139743274
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 503530
ClinVar RCV Id: RCV000591879
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361187.1:p.Gln536His
CA369588409
NM_001374258.1:c.1608A>C
CA369588410
NM_001374258.1:c.1608A>T