Canonical Allele Identifier: PA252040
Gene: UNC13D HGNC NCBI
ClinVar RCV:
RCV000002080
ClinVar Variation:
2003
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954712.1:p.Phe857Cys
CA252038
NM_199242.3:c.2570T>G