Canonical Allele Identifier: PA658808900
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_055240.2:p.Gly456Arg
CA197187603
NM_014425.5:c.1366G>C
CA374364888
NM_014425.5:c.1366G>A