Canonical Allele Identifier: PA2742023837
Gene: UBN2 HGNC NCBI
ClinVar RCV:
RCV004321594
ClinVar Variation:
2548576
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775840.3:p.Val226Ala
CA369405230
NM_173569.4:c.677T>C