Canonical Allele Identifier: PA2825295998
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 834382

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Arg1313Ser
CA133972240
NM_001008844.3:c.3939G>T
CA362689303
NM_001008844.3:c.3939G>C