Canonical Allele Identifier: PA645435766
Gene: IHH HGNC NCBI

Linked Data

ClinVar Variation Id: 286350
ClinVar RCV Id: RCV000367731
ClinVar Variation Id: 334444
ClinVar RCV Id: RCV000348092 RCV002521396
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002172.2:p.Arg77Ser
CA2116748
NM_002181.4:c.229C>A
CA10605437
NM_002181.4:c.228_229delinsAA