Canonical Allele Identifier: PA658676153
Gene: UNC93B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 470491

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_112192.2:p.Val485Met
CA6145375
NM_030930.4:c.1453G>A