Canonical Allele Identifier: PA111527
Gene: AGPS HGNC NCBI

Linked Data

ClinVar Variation Id: 35469
ClinVar RCV Id: RCV000029144
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003650.1:p.Thr568Met
CA129916
NM_003659.4:c.1703C>T