Canonical Allele Identifier: PA302317
Gene: SNTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 190929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003089.1:p.Phe130Leu
CA302315
NM_003098.3:c.388T>C
CA408633513
NM_003098.3:c.390T>G
CA408633514
NM_003098.3:c.390T>A