Canonical Allele Identifier: PA351649
Gene: BVES HGNC NCBI

Linked Data

ClinVar Variation Id: 222033
ClinVar RCV Id: RCV000207494
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186492.1:p.Ser201Phe
CA351648
NM_001199563.2:c.602C>T