Canonical Allele Identifier: PA2827028906
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 920089
ClinVar RCV Id: RCV001178662

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Met1535Ile
CA362689728
NM_001319034.2:c.4605G>A
CA362689729
NM_001319034.2:c.4605G>C
CA362689730
NM_001319034.2:c.4605G>T