Canonical Allele Identifier: PA245343
Gene: INVS HGNC NCBI

Linked Data

ClinVar Variation Id: 197295

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055240.2:p.Arg123Trp
CA245342
NM_014425.5:c.367C>T