Canonical Allele Identifier: PA2825316553
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_001013275.1:p.Arg77His
CA114284
NM_001013257.2:c.230G>A