Canonical Allele Identifier: PA2826990037
Gene: INVS HGNC NCBI

Linked Data

ClinVar Variation Id: 194407
ClinVar RCV Id: RCV000174771 RCV001084833 RCV003947476
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305310.1:p.Asp675Asn
CA240334
NM_001318381.2:c.2023G>A