Canonical Allele Identifier: PA2826990610
Gene: INVS HGNC NCBI

Linked Data

ClinVar Variation Id: 215514
ClinVar RCV Id: RCV000196500 RCV000378702 RCV001166462 RCV003430754
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305311.1:p.His609Tyr
CA336473
NM_001318382.2:c.1825C>T