Canonical Allele Identifier: PA2827028612
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 626739
ClinVar RCV Id: RCV000770237 RCV002533957
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Arg1308Leu
CA362685150
NM_001319034.2:c.3923G>T