Canonical Allele Identifier: PA2825870770
Gene: SLC30A7 HGNC NCBI

Linked Data

ClinVar Variation Id: 375382
ClinVar RCV Id: RCV000416450
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138356.1:p.His164Ser
CA16044212
NM_001144884.1:c.490_491delinsAG