Canonical Allele Identifier: PA354782
Gene: DISP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 218820
ClinVar RCV Id: RCV000203143

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116279.2:p.Ser1398Asn
CA249345
NM_032890.5:c.4193G>A