Canonical Allele Identifier: PA2827028850
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 3070068
ClinVar RCV Id: RCV004010100

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Gln1493His
CA045802
NM_001319034.2:c.4479G>C
CA362689456
NM_001319034.2:c.4479G>T