Canonical Allele Identifier: PA336474
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_055240.2:p.His935Tyr
CA336473
NM_014425.5:c.2803C>T