Canonical Allele Identifier: PA103605
Gene: IHH HGNC NCBI

Linked Data

ClinVar Variation Id: 8866

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002172.2:p.Glu95Lys
CA119973
NM_002181.4:c.283G>A