Canonical Allele Identifier: PA2826176057
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 1766498
ClinVar RCV Id: RCV002371539

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180233.1:p.Leu31Pro
CA347656128
NM_001193304.3:c.92T>C