Canonical Allele Identifier: PA2573237708
Gene: DSP HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Arg2826Ser
CA362695226
NM_004415.4:c.8476C>A