Canonical Allele Identifier: PA174266
Gene: SLC46A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 161525
ClinVar RCV Id: RCV000149060
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129391.1:p.Val397Ile
CA174265
NM_001135919.2:c.1189G>A