Canonical Allele Identifier: PA2826002165
Gene: PYGM HGNC NCBI

Linked Data

ClinVar Variation Id: 1306985
ClinVar RCV Id: RCV001772443 RCV002544018
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158188.1:p.Gly540Arg
CA6079685
NM_001164716.1:c.1618G>A
CA381169145
NM_001164716.1:c.1618G>C