Canonical Allele Identifier: PA2580312019
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2186899
ClinVar RCV Id: RCV002611188

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Ala2806Val
CA362695106
NM_004415.4:c.8417C>T