Canonical Allele Identifier: PA2825964761
Gene: PYGL HGNC NCBI

Linked Data

ClinVar Variation Id: 2736111
ClinVar RCV Id: RCV003513626

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157412.1:p.Asp77del
CA614275203
NM_001163940.2:c.229_231del