Allele Registry

Canonical Allele Identifier: PA2580385588

Gene: TAF9B HGNC NCBI

ClinVar RCV:

RCV004104775

ClinVar Variation:

2247860

HGVS (amino-acid)	Matching Registered Transcripts
NP_057059.2:p.Pro13Ala	CA413724056 NM_015975.5:c.37C>G