Canonical Allele Identifier: PA183790
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 179136
ClinVar RCV Id: RCV000155921 RCV001188627 RCV003114305 RCV003998294
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Pro847Leu
CA005397
NM_004415.4:c.2540C>T