Canonical Allele Identifier: PA2825964894
Gene: PYGL HGNC NCBI

Linked Data

ClinVar Variation Id: 1103947

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157412.1:p.Thr627Ala
CA7183257
NM_001163940.2:c.1879A>G