Allele Registry

Canonical Allele Identifier: PA3057516096

Gene: IHH HGNC NCBI

ClinVar RCV:

RCV005127916

ClinVar Variation:

3649009

HGVS (amino-acid)	Matching Registered Transcripts
NP_002172.2:p.Asp100His	CA350636653 NM_002181.4:c.298G>C