Canonical Allele Identifier: PA103597
Gene: IHH HGNC NCBI

Linked Data

ClinVar Variation Id: 8867
ClinVar RCV Id: RCV000009417
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002172.2:p.Glu131Lys
CA119974
NM_002181.4:c.391G>A