Canonical Allele Identifier: PA1139751599
Gene: SLC39A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 990600
ClinVar RCV Id: RCV001278658
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570901.3:p.Thr373Ser
CA4941398
NM_130849.4:c.1118C>G
CA372621134
NM_130849.4:c.1117A>T