Canonical Allele Identifier: PA2827028289
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 180327
ClinVar RCV Id: RCV000157194
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Ala1067Ser
CA005770
NM_001319034.2:c.3199G>T