Allele Registry

Canonical Allele Identifier: PA2499260592

Gene: IHH HGNC NCBI

ClinVar RCV:

RCV001582341

ClinVar Variation:

1217222

HGVS (amino-acid)	Matching Registered Transcripts
NP_002172.2:p.Arg160Cys	CA350634584 NM_002181.4:c.478C>T