Canonical Allele Identifier: PA1139717969
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 923727
ClinVar RCV Id: RCV001184648
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Arg1269Leu
CA362684894
NM_004415.4:c.3806G>T