Canonical Allele Identifier: PA2829889379
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 2784924
ClinVar RCV Id: RCV003633847

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060319.1:p.Gln168His
CA347652676
NM_017849.4:c.504G>T
CA347652679
NM_017849.4:c.504G>C