Canonical Allele Identifier: PA2573237723
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1392248
ClinVar RCV Id: RCV001896122
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Ser2861Phe
CA362695427
NM_004415.4:c.8582C>T