Canonical Allele Identifier: PA1139717517
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 927425
ClinVar RCV Id: RCV001190723

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Tyr1065Phe
CA362683268
NM_004415.4:c.3194A>T