Canonical Allele Identifier: PA916060344
Gene: SLC39A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 362237
ClinVar RCV Id: RCV000336853

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570901.3:p.Val384Met
CA10630457
NM_130849.4:c.1150G>A