Canonical Allele Identifier: PA2826990174
Gene: INVS HGNC NCBI

Linked Data

ClinVar Variation Id: 289200

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305310.1:p.Leu849His
CA5158723
NM_001318381.2:c.2546T>A