Canonical Allele Identifier: PA2827028386
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1000822
ClinVar RCV Id: RCV001297009 RCV003532929 RCV004004969
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Trp1155Cys
CA362684119
NM_001319034.2:c.3465G>T
CA362684121
NM_001319034.2:c.3465G>C