Canonical Allele Identifier: PA2828778634
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 375940
ClinVar RCV Id: RCV000440177
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365401.1:p.Val548Arg
CA16021333
NM_001378472.1:c.1642_1643delinsAG
CA645544098
NM_001378472.1:c.1642_1643delinsCG
CA645544099
NM_001378472.1:c.1641_1643delinsGAG