Canonical Allele Identifier: PA2826989783
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_001305310.1:p.Ser275Gly
CA5158332
NM_001318381.2:c.823A>G