Canonical Allele Identifier: PA2826176431
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 486548
ClinVar RCV Id: RCV000569055 RCV000806090 RCV002291674
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180233.1:p.Ser176Gly
CA347652535
NM_001193304.3:c.526A>G