Canonical Allele Identifier: PA2826990276
Gene: INVS HGNC NCBI

Linked Data

ClinVar Variation Id: 502745
ClinVar RCV Id: RCV000592544 RCV004024870
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305311.1:p.Gly130Arg
CA197187603
NM_001318382.2:c.388G>C
CA374364888
NM_001318382.2:c.388G>A