Canonical Allele Identifier: PA1139700819
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 923617
ClinVar RCV Id: RCV001184444
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Ser2644Thr
CA362694087
NM_004415.4:c.7931G>C