Canonical Allele Identifier: PA161379
Gene: PBRM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 135006
ClinVar RCV Id: RCV000121773
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060783.3:p.Tyr366Cys
CA161378
NM_018313.5:c.1097A>G