Canonical Allele Identifier: PA2826002239
Gene: PYGM HGNC NCBI

Linked Data

ClinVar Variation Id: 139609
ClinVar RCV Id: RCV000128553

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158188.1:p.Phe622del
CA345698
NM_001164716.1:c.1864_1866del