Canonical Allele Identifier: PA2826176563
Gene: TMEM127 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180233.1:p.Gln229Lys
CA347651122
NM_001193304.3:c.685C>A