Canonical Allele Identifier: PA2827029977
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 919071
ClinVar RCV Id: RCV001176997 RCV002555467
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Met2376Val
CA362695186
NM_001319034.2:c.7126A>G