Allele Registry

Canonical Allele Identifier: PA645435631

Gene: RFXAP HGNC NCBI

ClinVar RCV:

RCV000308335

ClinVar Variation:

311783

HGVS (amino-acid)	Matching Registered Transcripts
NP_000529.1:p.Pro26Arg	CA6950170 NM_000538.4:c.77C>G