Canonical Allele Identifier: PA2830186144
Gene: SLC39A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3164685
ClinVar RCV Id: RCV004461555

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570901.3:p.Phe414Leu
CA4941319
NM_130849.4:c.1240T>C
CA372619757
NM_130849.4:c.1242C>G
CA372619760
NM_130849.4:c.1242C>A