Canonical Allele Identifier: PA891854429
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 582892
ClinVar RCV Id: RCV000707080

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060319.1:p.Ala34Asp
CA347656112
NM_017849.4:c.101C>A