Canonical Allele Identifier: PA916022450
Gene: INVS HGNC NCBI

Linked Data

ClinVar Variation Id: 197295
ClinVar RCV Id: RCV000178293 RCV001089273 RCV003907613
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305310.1:p.Arg27Trp
CA245342
NM_001318381.2:c.79C>T