Canonical Allele Identifier: PA2825296067
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 3072758
ClinVar RCV Id: RCV004013780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Val1362Ala
CA362689620
NM_001008844.3:c.4085T>C