Canonical Allele Identifier: PA1139701530
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 919071

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Met2819Val
CA362695186
NM_004415.4:c.8455A>G