Canonical Allele Identifier: PA2827028458
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1733164
ClinVar RCV Id: RCV002455277

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Met1203Leu
CA362684447
NM_001319034.2:c.3607A>C
CA362684449
NM_001319034.2:c.3607A>T