Canonical Allele Identifier: PA916022461
Gene: INVS HGNC NCBI

Linked Data

ClinVar Variation Id: 199130
ClinVar RCV Id: RCV000180643
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305311.1:p.Thr66Ile
CA248163
NM_001318382.2:c.197C>T