Canonical Allele Identifier: PA2826990616
Gene: INVS HGNC NCBI

Linked Data

ClinVar Variation Id: 281735
ClinVar RCV Id: RCV000377481 RCV001336187 RCV001855089
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305311.1:p.His615Arg
CA10603960
NM_001318382.2:c.1844A>G