Canonical Allele Identifier: PA103614
Gene: IHH HGNC NCBI

Linked Data

ClinVar Variation Id: 8870
ClinVar RCV Id: RCV000009420

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002172.2:p.Pro46Leu
CA119977
NM_002181.4:c.137C>T