Canonical Allele Identifier: PA302260
Gene: SNTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 190909
ClinVar RCV Id: RCV000171092 RCV000765488 RCV001852056 RCV003298203
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003089.1:p.Phe176Leu
CA302258
NM_003098.3:c.526T>C
CA408632822
NM_003098.3:c.528C>G
CA408632824
NM_003098.3:c.528C>A