Canonical Allele Identifier: PA135228
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 44891
ClinVar RCV Id: RCV000038026 RCV000641814 RCV003531932 RCV004017317
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Ala1047Val
CA005749
NM_004415.4:c.3140C>T