Canonical Allele Identifier: PA2825296073
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 465901

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Leu1367Val
CA362689650
NM_001008844.3:c.4099C>G