Canonical Allele Identifier: PA2825296869
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 163287
ClinVar RCV Id: RCV000150581 RCV000157210 RCV000245063 RCV000262145 RCV000319713 RCV000369032 RCV000490472 RCV000771821 RCV000987654 RCV001086541 RCV001704081 RCV003945184 RCV003318355
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Arg2040Gln
CA007320
NM_001008844.3:c.6119G>A