Canonical Allele Identifier: PA645510468
Gene: IHH HGNC NCBI

Linked Data

ClinVar Variation Id: 273383
ClinVar RCV Id: RCV000508633

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002172.2:p.Gln51Lys
CA350637272
NM_002181.4:c.151C>A