Allele Registry

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Canonical Allele Identifier: PA1139751632

Gene: SLC39A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 910707

ClinVar RCV Id: RCV001162686

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_570901.3:p.Gly409Arg	CA372619857 NM_130849.4:c.1225G>C CA372619859 NM_130849.4:c.1225G>A