Canonical Allele Identifier: PA645435887
Gene: IHH HGNC NCBI

Linked Data

ClinVar Variation Id: 334439
ClinVar RCV Id: RCV000293234 RCV000967825
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002172.2:p.His252Arg
CA2116616
NM_002181.4:c.755A>G