Canonical Allele Identifier: PA302314
Gene: SNTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 190928

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003089.1:p.Ala122Thr
CA302312
NM_003098.3:c.364G>A