Canonical Allele Identifier: PA2826990400
Gene: INVS HGNC NCBI

Linked Data

ClinVar Variation Id: 220405
ClinVar RCV Id: RCV000206479 RCV001095342 RCV000595326 RCV003937782
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305311.1:p.Val323Met
CA350505
NM_001318382.2:c.967G>A