Canonical Allele Identifier: PA114285
Gene: BCAM HGNC NCBI
ClinVar RCV:
RCV000000467
ClinVar Variation:
438
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Amino-acid Alleles

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