Canonical Allele Identifier: PA2827027355
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1776292
ClinVar RCV Id: RCV002400869
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Tyr350Ser
CA362675457
NM_001319034.2:c.1049A>C