Canonical Allele Identifier: PA2829969157
Gene: PSAT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 976987
ClinVar Variation Id: 976988
ClinVar RCV Id: RCV001254500

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066977.1:p.Lys116Asn
CA5095588
NM_021154.5:c.348G>C
CA373872482
NM_021154.5:c.348G>T