Canonical Allele Identifier: PA916056181
Gene: SLC39A4 HGNC NCBI
ClinVar RCV:
RCV000003718
ClinVar Variation:
3540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060237.3:p.Asn81Lys
CA116335
NM_017767.3:c.243C>A
CA372625390
NM_017767.3:c.243C>G