Canonical Allele Identifier: PA915971375
Gene: PYGL HGNC NCBI

Linked Data

ClinVar Variation Id: 655030
ClinVar RCV Id: RCV000811116
ClinVar Variation Id: 1685053

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002854.3:p.Gly691Arg
CA7183229
NM_002863.5:c.2071G>A
CA7183230
NM_002863.5:c.2071G>C