Canonical Allele Identifier: PA2825803396
Gene: SLC46A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2277495
ClinVar RCV Id: RCV004127126
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129391.1:p.Cys141Gly
CA387804448
NM_001135919.2:c.421T>G