Canonical Allele Identifier: PA2829880438
Gene: SLC39A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 990600
ClinVar RCV Id: RCV001278658

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060237.3:p.Thr348Ser
CA4941398
NM_017767.3:c.1043C>G
CA372621134
NM_017767.3:c.1042A>T