Allele Registry

Canonical Allele Identifier: PA2499270771

Gene: H3-3B HGNC NCBI

ClinVar RCV:

RCV001541919

RCV001823781

ClinVar Variation:

1183984

HGVS (amino-acid)	Matching Registered Transcripts
NP_005315.1:p.Ile52Asn	CA401117707 NM_005324.5:c.155T>A