Canonical Allele Identifier: PA2828776691
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1691521
ClinVar RCV Id: RCV002254850
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365398.1:p.Met598Val
CA369542712
NM_001378469.1:c.1792A>G