Canonical Allele Identifier: PA174580
Gene: GAPDHS HGNC NCBI

Linked Data

ClinVar Variation Id: 161676
ClinVar RCV Id: RCV000149212
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055179.1:p.Asp377Asn
CA174579
NM_014364.5:c.1129G>A