Canonical Allele Identifier: PA1139719383
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 920089
ClinVar RCV Id: RCV001178662

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Met1978Ile
CA362689728
NM_004415.4:c.5934G>A
CA362689729
NM_004415.4:c.5934G>C
CA362689730
NM_004415.4:c.5934G>T