Canonical Allele Identifier: PA2829968902
Gene: PSAT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1492981
ClinVar RCV Id: RCV001984019

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066977.1:p.Leu40Val
CA373871615
NM_021154.5:c.118C>G