ClinGen Allele Registry
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Canonical Allele Identifier:
PA2829880048
Gene: SLC39A4
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000003722
RCV002512719
ClinVar Variation:
3544
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_060237.3:p.Arg70Cys
CA116339
NM_017767.3:c.208C>T