Canonical Allele Identifier: PA2829546738
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 3075276
ClinVar RCV Id: RCV004015802

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Thr2775Ser
CA362694915
NM_004415.4:c.8323A>T
CA362694917
NM_004415.4:c.8324C>G