Canonical Allele Identifier: PA2825964941
Gene: PYGL HGNC NCBI

Linked Data

ClinVar Variation Id: 258843
ClinVar RCV Id: RCV000244701 RCV000353747 RCV000675360
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157412.1:p.Asn811Ser
CA7183086
NM_001163940.2:c.2432A>G