Canonical Allele Identifier: PA1139757949
Gene: PSAT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 977035
ClinVar RCV Id: RCV001254554
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478059.1:p.Leu128Phe
CA5095594
NM_058179.4:c.382C>T