Canonical Allele Identifier: PA082740
Gene: TMEM199 HGNC NCBI

Linked Data

ClinVar Variation Id: 218964
ClinVar RCV Id: RCV000208697 RCV000210790 RCV002517364 RCV003407721
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689677.1:p.Arg31Pro
CA082736
NM_152464.3:c.92G>C