Canonical Allele Identifier: PA2825964909
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_001157412.1:p.Gly657Arg
CA7183229
NM_001163940.2:c.1969G>A
CA7183230
NM_001163940.2:c.1969G>C