Canonical Allele Identifier: PA2828775990
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 375944
ClinVar RCV Id: RCV000428481 RCV000824926
ClinVar Variation Id: 375945
ClinVar RCV Id: RCV000438728
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365397.1:p.Asp594Glu
CA16602423
NM_001378468.1:c.1782T>G
CA16602424
NM_001378468.1:c.1782T>A