Canonical Allele Identifier: PA2826176337
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 824428
ClinVar RCV Id: RCV001021524

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180233.1:p.Ala132Val
CA347653274
NM_001193304.3:c.395C>T