Canonical Allele Identifier: PA2580415942
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 1766498
ClinVar RCV Id: RCV002371539

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060319.1:p.Leu31Pro
CA347656128
NM_017849.4:c.92T>C