Canonical Allele Identifier: PA645469818
Gene: INVS HGNC NCBI

Linked Data

ClinVar Variation Id: 364221
ClinVar RCV Id: RCV000399541 RCV000734866 RCV001448682 RCV003912559
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055240.2:p.Leu40Val
CA5158084
NM_014425.5:c.118C>G