Allele Registry

Canonical Allele Identifier: PA2580361092

Gene: IPO13 HGNC NCBI

ClinVar RCV:

RCV004087923

ClinVar Variation:

2221171

HGVS (amino-acid)	Matching Registered Transcripts
NP_055467.3:p.Arg847Trp	CA815669 NM_014652.4:c.2539C>T