Canonical Allele Identifier: PA2828700999
Gene: DISP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 218820
ClinVar RCV Id: RCV000203143

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364158.1:p.Ser1398Asn
CA249345
NM_001377229.1:c.4193G>A