Canonical Allele Identifier: PA114285
Gene: BCAM HGNC NCBI

Linked Data

ClinVar Variation Id: 438
ClinVar RCV Id: RCV000000467
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005572.2:p.Arg77His
CA114284
NM_005581.5:c.230G>A