Allele Registry

Canonical Allele Identifier: PA645423559

Gene: TMEM47 HGNC NCBI

ClinVar RCV:

RCV000491018

ClinVar Variation:

242889

HGVS (amino-acid)	Matching Registered Transcripts
NP_113630.1:p.Arg12Pro	CA412682009 NM_031442.4:c.35G>C