Canonical Allele Identifier: PA1139717818
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 948741
ClinVar RCV Id: RCV001220053
ClinVar Variation Id: 2925027
ClinVar RCV Id: RCV003780681
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Glu1191Asp
CA038437
NM_004415.4:c.3573G>C
CA362684370
NM_004415.4:c.3573G>T