Canonical Allele Identifier: PA915967490
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 646527
ClinVar RCV Id: RCV000800825

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Ser1127Pro
CA362683872
NM_004415.4:c.3379T>C