Canonical Allele Identifier: PA2825295978
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 952754
ClinVar RCV Id: RCV001224923 RCV001526201
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Leu1296Val
CA362689181
NM_001008844.3:c.3886C>G