Canonical Allele Identifier: PA1139700692
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 926948
ClinVar RCV Id: RCV001189858

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Leu2613Pro
CA362693888
NM_004415.4:c.7838T>C