Canonical Allele Identifier: PA2825964898
Gene: PYGL HGNC NCBI

Linked Data

ClinVar Variation Id: 21332
ClinVar RCV Id: RCV000020497

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157412.1:p.Glu639Lys
CA341912
NM_001163940.2:c.1915G>A