Canonical Allele Identifier: PA2826989725
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_001305310.1:p.His176Pro
CA5158255
NM_001318381.2:c.527A>C