Canonical Allele Identifier: PA2826989792
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_001305310.1:p.Thr296Ile
CA248163
NM_001318381.2:c.887C>T