Allele Registry

Canonical Allele Identifier: PA238540

Gene: CRH HGNC NCBI

ClinVar RCV:

RCV000172993

RCV000192059

RCV004019949

ClinVar Variation:

183027

HGVS (amino-acid)	Matching Registered Transcripts
NP_000747.1:p.Pro30Arg	CA238539 NM_000756.2:c.89C>G