Canonical Allele Identifier: PA240126
Gene: INVS HGNC NCBI

Linked Data

ClinVar Variation Id: 194250

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055240.2:p.Lys642Arg
CA240125
NM_014425.5:c.1925A>G