Allele Registry

Canonical Allele Identifier: PA137764

Gene: TMEM43 HGNC NCBI

ClinVar RCV:

RCV000030555

RCV000039394

RCV000243225

RCV000336793

RCV000756785

RCV001528963

RCV002490427

ClinVar Variation:

36873

HGVS (amino-acid)	Matching Registered Transcripts
NP_077310.1:p.Arg312Trp	CA024800 NM_024334.3:c.934C>T