Canonical Allele Identifier: PA658676227
Gene: UNC13D HGNC NCBI

Linked Data

ClinVar Variation Id: 464450
ClinVar RCV Id: RCV000558264
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954712.1:p.Ala461Val
CA8773012
NM_199242.3:c.1382C>T