Canonical Allele Identifier: PA2573220605
Gene: IHH HGNC NCBI

Linked Data

ClinVar Variation Id: 1445393
ClinVar RCV Id: RCV001985018
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002172.2:p.Pro54Ser
CA350637205
NM_002181.4:c.160C>T