Canonical Allele Identifier: PA645461685
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 432555
ClinVar RCV Id: RCV000498892

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Leu2077Val
CA047115
NM_004415.4:c.6229C>G