Canonical Allele Identifier: PA2826990164
Gene: INVS HGNC NCBI

Linked Data

ClinVar Variation Id: 215514
ClinVar RCV Id: RCV000196500 RCV000378702 RCV001166462 RCV003430754
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305310.1:p.His839Tyr
CA336473
NM_001318381.2:c.2515C>T