Canonical Allele Identifier: PA2580380099
Gene: INTU HGNC NCBI

Linked Data

ClinVar Variation Id: 1986417
ClinVar RCV Id: RCV002786174 RCV002786173
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056508.2:p.Val209Met
CA3074828
NM_015693.3:c.625G>A