Canonical Allele Identifier: PA2573237151
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1410800
ClinVar RCV Id: RCV001920295

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Met1299Ile
CA362685094
NM_004415.4:c.3897G>A
CA362685095
NM_004415.4:c.3897G>C
CA362685096
NM_004415.4:c.3897G>T