Canonical Allele Identifier: PA1139719267
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 834382

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Arg1912Ser
CA133972240
NM_004415.4:c.5736G>T
CA362689303
NM_004415.4:c.5736G>C