Canonical Allele Identifier: PA2741890418
Gene: IHH HGNC NCBI

Linked Data

ClinVar Variation Id: 3006505
ClinVar RCV Id: RCV003866656
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002172.2:p.Asn55Ser
CA2116761
NM_002181.4:c.164A>G