Canonical Allele Identifier: PA2580374642
Gene: SLC39A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2458365
ClinVar RCV Id: RCV004254636

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036451.4:p.His523Arg
CA8939047
NM_012319.4:c.1568A>G