Allele Registry

Canonical Allele Identifier: PA2580285601

Gene: H4C9 HGNC NCBI

ClinVar RCV:

RCV003152474

ClinVar Variation:

2443866

HGVS (amino-acid)	Matching Registered Transcripts
NP_003486.1:p.His76Arg	CA363244654 NM_003495.3:c.227A>G