Canonical Allele Identifier: PA658808899
Gene: INVS HGNC NCBI

Linked Data

ClinVar Variation Id: 531619
ClinVar RCV Id: RCV000729967 RCV001089255 RCV001166924 RCV003258899
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055240.2:p.Ser371Gly
CA5158332
NM_014425.5:c.1111A>G