Canonical Allele Identifier: PA2828778522
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13978
ClinVar RCV Id: RCV000015012 RCV000211750 RCV000207518 RCV000414915 RCV000808147 RCV001273349
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365401.1:p.Glu449Gly
CA279974
NM_001378472.1:c.1346A>G