Canonical Allele Identifier: PA2826176369
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 2679214
ClinVar RCV Id: RCV003466446

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180233.1:p.Gly145Ser
CA347653103
NM_001193304.3:c.433G>A