Canonical Allele Identifier: PA2741923601
Gene: PYGM HGNC NCBI

Linked Data

ClinVar Variation Id: 2547500
ClinVar RCV Id: RCV003257633

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005600.1:p.Tyr778Asp
CA381164515
NM_005609.4:c.2332T>G