Canonical Allele Identifier: PA1139717843
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 926130
ClinVar RCV Id: RCV001188522

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Lys1209Arg
CA362684496
NM_004415.4:c.3626A>G