Allele Registry

Canonical Allele Identifier: PA103578

Gene: IHH HGNC NCBI

ClinVar RCV:

RCV000009419

RCV001804721

RCV003441711

ClinVar Variation:

8869

HGVS (amino-acid)	Matching Registered Transcripts
NP_002172.2:p.Asp100Asn	CA119976 NM_002181.4:c.298G>A