Canonical Allele Identifier: PA2826990010
Gene: INVS HGNC NCBI

Linked Data

ClinVar Variation Id: 289548
ClinVar RCV Id: RCV000393475 RCV000638082 RCV002502150
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305310.1:p.Arg638Trp
CA5158579
NM_001318381.2:c.1912C>T