Canonical Allele Identifier: PA2829543587
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 3071469
ClinVar RCV Id: RCV004015963

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Asn274His
CA362674151
NM_004415.4:c.820A>C