Canonical Allele Identifier: PA1139715226
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 923801
ClinVar RCV Id: RCV001184794 RCV002339468 RCV003226437 RCV002559873 RCV004008482
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Arg39Ser
CA133980184
NM_004415.4:c.117G>T
CA362675859
NM_004415.4:c.117G>C