Canonical Allele Identifier: PA261239
Gene: PYGM HGNC NCBI
ClinVar RCV:
RCV000033140
ClinVar Variation:
40042
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158188.1:p.Asp51Gly
CA261238
NM_001164716.1:c.152A>G