Canonical Allele Identifier: PA2580272228
Gene: IHH HGNC NCBI

Linked Data

ClinVar Variation Id: 2166441
ClinVar RCV Id: RCV003091762

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002172.2:p.Val45Gly
CA2116767
NM_002181.4:c.134T>G