Canonical Allele Identifier: PA2825294921
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 3070921
ClinVar RCV Id: RCV004014423
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Ser457Asn
CA362676592
NM_001008844.3:c.1370G>A