Canonical Allele Identifier: PA2825295977
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1895478
ClinVar RCV Id: RCV002569461

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Ser1295Arg
CA362689172
NM_001008844.3:c.3883A>C
CA362689178
NM_001008844.3:c.3885T>A
CA362689179
NM_001008844.3:c.3885T>G