Canonical Allele Identifier: PA175942
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 161226
ClinVar RCV Id: RCV000148476 RCV000150560 RCV000284191 RCV000285554 RCV000515316 RCV000476727 RCV000617402 RCV000626864 RCV000771793 RCV000735747 RCV000766877 RCV003483521
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Ala566Thr
CA004119
NM_004415.4:c.1696G>A