Canonical Allele Identifier: PA658808890
Gene: INVS HGNC NCBI

Linked Data

ClinVar Variation Id: 497966
ClinVar RCV Id: RCV000596250 RCV002476286 RCV002532393
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055240.2:p.His272Pro
CA5158255
NM_014425.5:c.815A>C