Canonical Allele Identifier: PA1139701840
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 924961
ClinVar RCV Id: RCV001186628
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Gly2870Arg
CA362695485
NM_004415.4:c.8608G>A
CA362695486
NM_004415.4:c.8608G>C