Canonical Allele Identifier: PA658682112
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 463847

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060319.1:p.Val143Ile
CA1777304
NM_017849.4:c.427G>A