Canonical Allele Identifier: PA2825296465
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 222583
ClinVar RCV Id: RCV000208472 RCV003765343
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Thr1688Ser
CA354024
NM_001008844.3:c.5062A>T
CA362691716
NM_001008844.3:c.5063C>G