Canonical Allele Identifier: PA2499283932
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 1014859

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060319.1:p.Tyr220His
CA347651492
NM_017849.4:c.658T>C