Canonical Allele Identifier: PA2827353894
Gene: TMEM121 HGNC NCBI

Linked Data

ClinVar Variation Id: 2344789
ClinVar RCV Id: RCV004184098

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001318167.1:p.Asn291His
CA7391503
NM_001331238.2:c.871A>C