Canonical Allele Identifier: PA2828777880
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1900738
ClinVar RCV Id: RCV002585865
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365400.1:p.Lys436Arg
CA369588858
NM_001378471.1:c.1307A>G