Canonical Allele Identifier: PA2499260589
Gene: IHH HGNC NCBI

Linked Data

ClinVar Variation Id: 1062126
ClinVar RCV Id: RCV001371806
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002172.2:p.Ala48Val
CA2116762
NM_002181.4:c.143C>T