Canonical Allele Identifier: PA658669597
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 465880
ClinVar RCV Id: RCV000530778 RCV003999164
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Arg464Ser
CA362676709
NM_004415.4:c.1392A>C
CA362676712
NM_004415.4:c.1392A>T