Canonical Allele Identifier: PA2829040165
Gene: CD19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2420507
ClinVar RCV Id: RCV003121672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372661.1:p.Met387Val
CA395406752
NM_001385732.1:c.1159A>G