Canonical Allele Identifier: PA2826002167
Gene: PYGM HGNC NCBI

Linked Data

ClinVar Variation Id: 1179912
ClinVar RCV Id: RCV001536996 RCV001826385
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158188.1:p.Asp541Tyr
CA6079684
NM_001164716.1:c.1621G>T