Canonical Allele Identifier: PA1139700743
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 978329

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Ser2617Asn
CA050983
NM_004415.4:c.7850G>A