Canonical Allele Identifier: PA2825297109
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2775383
ClinVar RCV Id: RCV003533791
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Met2194Ile
CA362695033
NM_001008844.3:c.6582G>A
CA362695034
NM_001008844.3:c.6582G>C
CA362695035
NM_001008844.3:c.6582G>T