Canonical Allele Identifier: PA2826001678
Gene: PYGM HGNC NCBI

Linked Data

ClinVar Variation Id: 2702114
ClinVar RCV Id: RCV003498270
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158188.1:p.Met1Ile
CA381113473
NM_001164716.1:c.3G>T
CA381113487
NM_001164716.1:c.3G>C
CA381113489
NM_001164716.1:c.3G>A