Canonical Allele Identifier: PA1139719261
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 920064
ClinVar RCV Id: RCV001178603 RCV003769929
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Ala1904Val
CA362689246
NM_004415.4:c.5711C>T