Canonical Allele Identifier: PA161368
Gene: PAX5 HGNC NCBI

Linked Data

ClinVar Variation Id: 135001

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057953.1:p.Ser213Leu
CA161367
NM_016734.3:c.638C>T