Allele Registry

Canonical Allele Identifier: PA2580402623

Gene: CHDH HGNC NCBI

ClinVar RCV:

RCV004072365

ClinVar Variation:

2204929

HGVS (amino-acid)	Matching Registered Transcripts
NP_060867.2:p.Ile299Val	CA2455740 NM_018397.5:c.895A>G