Canonical Allele Identifier: PA916004891
Gene: TRIM49B HGNC NCBI

Linked Data

ClinVar Variation Id: 776610
ClinVar RCV Id: RCV000956940
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193555.1:p.Met1Val