Canonical Allele Identifier: PA2499260590
Gene: IHH HGNC NCBI

Linked Data

ClinVar Variation Id: 1224454
ClinVar RCV Id: RCV001597521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002172.2:p.Phe91Leu
CA350636743
NM_002181.4:c.273C>G
CA350636744
NM_002181.4:c.273C>A
CA350636752
NM_002181.4:c.271T>C