Canonical Allele Identifier: PA2826176343
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 2750883
ClinVar RCV Id: RCV003516918

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180233.1:p.His133Tyr
CA347653271
NM_001193304.3:c.397C>T