Canonical Allele Identifier: PA2826002017
Gene: PYGM HGNC NCBI

Linked Data

ClinVar Variation Id: 2100385
ClinVar RCV Id: RCV003014369

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158188.1:p.His363_Ala369del
CA2580084649
NM_001164716.1:c.1088_1108del