Canonical Allele Identifier: PA2828556011
Gene: SLC39A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3164685
ClinVar RCV Id: RCV004461555

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361768.1:p.Phe320Leu
CA4941319
NM_001374839.1:c.958T>C
CA372619757
NM_001374839.1:c.960C>G
CA372619760
NM_001374839.1:c.960C>A