Canonical Allele Identifier: PA2827029624
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2453245
ClinVar RCV Id: RCV003182700
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Ser2140Arg
CA362693690
NM_001319034.2:c.6418A>C
CA362693696
NM_001319034.2:c.6420C>A
CA362693697
NM_001319034.2:c.6420C>G