Canonical Allele Identifier: PA2825297154
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 44968
ClinVar RCV Id: RCV000038105 RCV000172546 RCV000203133 RCV000392037 RCV000337923 RCV000620878 RCV000777790 RCV001095186 RCV001085488
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Met2220Leu
CA007553
NM_001008844.3:c.6658A>C
CA362695185
NM_001008844.3:c.6658A>T