Allele Registry

Canonical Allele Identifier: PA2741903269

Gene: H2BC8 HGNC NCBI

ClinVar RCV:

RCV004344540

ClinVar Variation:

2604945

HGVS (amino-acid)	Matching Registered Transcripts
NP_003509.1:p.Lys24Asn	CA363204375 NM_003518.4:c.72G>T CA363204379 NM_003518.4:c.72G>C