Canonical Allele Identifier: PA2827028816
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_001305963.1:p.Cys1470Ser
CA133972251
NM_001319034.2:c.4409G>C
CA362689304
NM_001319034.2:c.4408T>A