Canonical Allele Identifier: PA2825294699
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 228652
ClinVar RCV Id: RCV000221921
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Ser299Gly
CA10576693
NM_001008844.3:c.895A>G