Canonical Allele Identifier: PA2827555928
Gene: DISP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 218820
ClinVar RCV Id: RCV000203143

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337559.1:p.Ser1155Asn
CA249345
NM_001350630.2:c.3464G>A