Canonical Allele Identifier: PA2827029020
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2940821
ClinVar RCV Id: RCV003800131
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Thr1625Ser
CA362690297
NM_001319034.2:c.4873A>T
CA362690300
NM_001319034.2:c.4874C>G