Canonical Allele Identifier: PA2830185954
Gene: SLC39A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3540
ClinVar RCV Id: RCV000003718
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570901.3:p.Asn106Lys
CA116335
NM_130849.4:c.318C>A
CA372625390
NM_130849.4:c.318C>G