Canonical Allele Identifier: PA2826176213
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 2761287
ClinVar RCV Id: RCV003517118

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180233.1:p.Phe83Leu
CA347653709
NM_001193304.3:c.249C>G
CA347653710
NM_001193304.3:c.249C>A
CA347653736
NM_001193304.3:c.247T>C