Canonical Allele Identifier: PA915992831
Gene: PGM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 13650
ClinVar RCV Id: RCV000014620

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166289.1:p.Thr133Ala
CA123324
NM_001172818.1:c.397A>G