Canonical Allele Identifier: PA2826989692
Gene: INVS HGNC NCBI

Linked Data

ClinVar Variation Id: 1435322
ClinVar RCV Id: RCV001984869
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305310.1:p.Pro113Ser
CA5158210
NM_001318381.2:c.337C>T