Canonical Allele Identifier: PA2826002292
Gene: PYGM HGNC NCBI

Linked Data

ClinVar Variation Id: 2547500
ClinVar RCV Id: RCV003257633
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158188.1:p.Tyr690Asp
CA381164515
NM_001164716.1:c.2068T>G