Canonical Allele Identifier: PA2827353899
Gene: TMEM121 HGNC NCBI

Linked Data

ClinVar Variation Id: 2344323
ClinVar RCV Id: RCV004188478

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001318167.1:p.Ser311Leu
CA7391515
NM_001331238.2:c.932C>T