Canonical Allele Identifier: PA2580471507
Gene: TMEM121 HGNC NCBI

Linked Data

ClinVar Variation Id: 2257231
ClinVar RCV Id: RCV004110919

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079544.1:p.Leu317Arg
CA391203821
NM_025268.4:c.950T>G