Canonical Allele Identifier: PA645461055
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 228652
ClinVar RCV Id: RCV000221921

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Ser299Gly
CA10576693
NM_004415.4:c.895A>G