Canonical Allele Identifier: PA2827353901
Gene: TMEM121 HGNC NCBI

Linked Data

ClinVar Variation Id: 2257231
ClinVar RCV Id: RCV004110919

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001318167.1:p.Leu317Arg
CA391203821
NM_001331238.2:c.950T>G