Canonical Allele Identifier: PA1139701301
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 928301
ClinVar RCV Id: RCV001192077
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Val2741Met
CA051822
NM_004415.4:c.8221G>A