Canonical Allele Identifier: PA2741910569
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2947917
ClinVar RCV Id: RCV003806739
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Ala1044Val
CA037206
NM_004415.4:c.3131C>T