Canonical Allele Identifier: PA114287
Gene: BCAM HGNC NCBI

Linked Data

ClinVar Variation Id: 439
ClinVar RCV Id: RCV000000468 RCV002496219 RCV003964784
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005572.2:p.Thr539Ala
CA114286
NM_005581.5:c.1615A>G