Canonical Allele Identifier: PA913193681
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 626739
ClinVar RCV Id: RCV000770237 RCV002533957
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Arg1308Leu
CA362685150
NM_004415.4:c.3923G>T