Canonical Allele Identifier: PA658669922
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 465902
ClinVar RCV Id: RCV000621387 RCV000546727 RCV000825753 RCV001181858 RCV001547589
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Val2004Phe
CA046586
NM_004415.4:c.6010G>T