Canonical Allele Identifier: PA1139700030
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 926990
ClinVar RCV Id: RCV001189944 RCV001205397 RCV002375104
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Glu2400Asp
CA362692460
NM_004415.4:c.7200A>C
CA362692461
NM_004415.4:c.7200A>T