Canonical Allele Identifier: PA645411760
Gene: PYGL HGNC NCBI

Linked Data

ClinVar Variation Id: 313320
ClinVar RCV Id: RCV000378008

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002854.3:p.Leu739Met
CA7183172
NM_002863.5:c.2215C>A