Canonical Allele Identifier: PA2825297092
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2775382
ClinVar RCV Id: RCV003533790 RCV003779371 RCV004011644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Leu2182Phe
CA052088
NM_001008844.3:c.6546A>T
CA362694957
NM_001008844.3:c.6546A>C