Canonical Allele Identifier: PA891857862
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 580092
ClinVar RCV Id: RCV000703536 RCV001163042 RCV001183567 RCV001163043 RCV001163044
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Asn1257Ser
CA362684816
NM_004415.4:c.3770A>G