Canonical Allele Identifier: PA2830186139
Gene: SLC39A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3164684
ClinVar RCV Id: RCV004461554
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570901.3:p.Gly409Glu
CA372619853
NM_130849.4:c.1226G>A