Canonical Allele Identifier: PA174774
Gene: USP48 HGNC NCBI

Linked Data

ClinVar Variation Id: 161781
ClinVar RCV Id: RCV000149317
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115612.4:p.Met415Val
CA174773
NM_032236.8:c.1243A>G