Canonical Allele Identifier: PA2827028783
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2938816
ClinVar RCV Id: RCV003799590 RCV004006049
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Ser1445Arg
CA362689128
NM_001319034.2:c.4333A>C
CA362689134
NM_001319034.2:c.4335T>A
CA362689135
NM_001319034.2:c.4335T>G