Canonical Allele Identifier: PA916022460
Gene: INVS HGNC NCBI

Linked Data

ClinVar Variation Id: 531619
ClinVar RCV Id: RCV000729967 RCV001089255 RCV001166924 RCV003258899
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305311.1:p.Ser45Gly
CA5158332
NM_001318382.2:c.133A>G