Canonical Allele Identifier: PA2580543537
Gene: DPY19L2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2399143
ClinVar RCV Id: RCV002749559

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_776173.3:p.Ala487Val
CA6665504
NM_173812.5:c.1460C>T