Canonical Allele Identifier: PA913193652
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 629369

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Asn1051Lys
CA362683133
NM_004415.4:c.3153C>G
CA362683135
NM_004415.4:c.3153C>A