Canonical Allele Identifier: PA1139701526
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 920083
ClinVar RCV Id: RCV001178655
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Pro2814Ser
CA362695150
NM_004415.4:c.8440C>T