Canonical Allele Identifier: PA1139717411
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 920654
ClinVar RCV Id: RCV001179510 RCV001875940 RCV002491519
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Leu1007Phe
CA133965889
NM_004415.4:c.3019C>T