Canonical Allele Identifier: PA2826745774
Gene: FPGS HGNC NCBI

Linked Data

ClinVar Variation Id: 2374951
ClinVar RCV Id: RCV004213072
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001275732.1:p.Ala477Thr
CA5252503
NM_001288803.1:c.1429G>A