Canonical Allele Identifier: PA2826001705
Gene: PYGM HGNC NCBI

Linked Data

ClinVar Variation Id: 305285
ClinVar RCV Id: RCV000290610

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158188.1:p.Asn33Ser
CA10638975
NM_001164716.1:c.98A>G