Canonical Allele Identifier: PA2741910824
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2938816

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Ser1888Arg
CA362689128
NM_004415.4:c.5662A>C
CA362689134
NM_004415.4:c.5664T>A
CA362689135
NM_004415.4:c.5664T>G