Canonical Allele Identifier: PA135084
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 44802
ClinVar RCV Id: RCV000037918
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004324.2:p.Gly469del
CA135082
NM_004333.6:c.1405_1407del