Canonical Allele Identifier: PA2829730228
Gene: SLC39A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 3164720
ClinVar RCV Id: RCV004461590

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036451.4:p.Pro533Leu
CA8939041
NM_012319.4:c.1598C>T