Canonical Allele Identifier: PA2580272225
Gene: IHH HGNC NCBI

Linked Data

ClinVar Variation Id: 1997818
ClinVar RCV Id: RCV002791965
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002172.2:p.Gly35Asp
CA2116773
NM_002181.4:c.104G>A