Canonical Allele Identifier: PA1139728268
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 960997
ClinVar RCV Id: RCV001234621 RCV002451562
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060319.1:p.His120Arg
CA1777345
NM_017849.4:c.359A>G