Canonical Allele Identifier: PA2828779090
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40367
ClinVar RCV Id: RCV000033308 RCV000417719 RCV000654957 RCV002051798
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365402.1:p.Val419Phe
CA281968
NM_001378473.1:c.1255G>T