Canonical Allele Identifier: PA2826002281
Gene: PYGM HGNC NCBI

Linked Data

ClinVar Variation Id: 2075803
ClinVar RCV Id: RCV002967974

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158188.1:p.His681Pro
CA6079573
NM_001164716.1:c.2042A>C