Canonical Allele Identifier: PA2825667262
Gene: SLC39A13 HGNC NCBI
ClinVar RCV:
RCV003204683
ClinVar Variation:
2481815
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121697.2:p.Met11Thr
CA380308581
NM_001128225.3:c.32T>C