Canonical Allele Identifier: PA2499267786
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1041718

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Thr2798Ser
CA133977951
NM_004415.4:c.8392A>T
CA362695063
NM_004415.4:c.8393C>G