Canonical Allele Identifier: PA2580282564
Gene: SNTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1735691
ClinVar RCV Id: RCV002355605

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003089.1:p.Leu129Pro
CA408633520
NM_003098.3:c.386T>C