Canonical Allele Identifier: PA346294
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 180327
ClinVar RCV Id: RCV000157194
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Ala1067Ser
CA005770
NM_004415.4:c.3199G>T