Canonical Allele Identifier: PA2827028453
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 191639
ClinVar RCV Id: RCV000171914 RCV000693151 RCV001523968 RCV002453593 RCV003387786
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Asn1200Lys
CA004249
NM_001319034.2:c.3600T>G
CA362684432
NM_001319034.2:c.3600T>A