Canonical Allele Identifier: PA2826001704
Gene: PYGM HGNC NCBI

Linked Data

ClinVar Variation Id: 3150216
ClinVar RCV Id: RCV004440639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158188.1:p.Asn33Lys
CA381112886
NM_001164716.1:c.99C>G
CA381112889
NM_001164716.1:c.99C>A