Canonical Allele Identifier: PA2828778298
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 2633111
ClinVar RCV Id: RCV003408428
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365401.1:p.Phe238Leu
CA369590537
NM_001378472.1:c.714T>G
CA369590538
NM_001378472.1:c.714T>A
CA369590543
NM_001378472.1:c.712T>C