Canonical Allele Identifier: PA645470668
Gene: AGPS HGNC NCBI

Linked Data

ClinVar Variation Id: 332510
ClinVar RCV Id: RCV000400035 RCV002521338
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003650.1:p.Ala22Gly
CA1980002
NM_003659.4:c.65C>G