Canonical Allele Identifier: PA645470008
Gene: INVS HGNC NCBI

Linked Data

ClinVar Variation Id: 281735
ClinVar RCV Id: RCV000377481 RCV001336187 RCV001855089
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055240.2:p.His941Arg
CA10603960
NM_014425.5:c.2822A>G