Canonical Allele Identifier: PA2826002035
Gene: PYGM HGNC NCBI

Linked Data

ClinVar Variation Id: 1518551
ClinVar RCV Id: RCV002023942
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158188.1:p.His372Arg
CA381175711
NM_001164716.1:c.1115A>G