Canonical Allele Identifier: PA913193652
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 629369
ClinVar RCV Id: RCV000774071 RCV001034964 RCV002501003 RCV003480809 RCV004027261
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Asn1051Lys
CA362683133
NM_004415.4:c.3153C>G
CA362683135
NM_004415.4:c.3153C>A