Allele Registry

Canonical Allele Identifier: PA645510468

Gene: IHH HGNC NCBI

ClinVar RCV:

RCV000508633

ClinVar Variation:

273383

HGVS (amino-acid)	Matching Registered Transcripts
NP_002172.2:p.Gln51Lys	CA350637272 NM_002181.4:c.151C>A