Canonical Allele Identifier: PA2741910988
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2946437
ClinVar RCV Id: RCV003806723
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Glu2629Gly
CA362693990
NM_004415.4:c.7886A>G