Canonical Allele Identifier: PA1139710841
Gene: IHH HGNC NCBI

Linked Data

ClinVar Variation Id: 834083

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002172.2:p.Glu95del
CA350636701
NM_002181.4:c.283G>T
CA350636713
NM_002181.4:c.280G>T
CA1139657700
NM_002181.4:c.283_285del