Canonical Allele Identifier: PA2825295999
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 925788
ClinVar RCV Id: RCV001187954 RCV003770106 RCV004008752
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Cys1314Ser
CA133972251
NM_001008844.3:c.3941G>C
CA362689304
NM_001008844.3:c.3940T>A