Canonical Allele Identifier: PA2580123451
Gene: BCL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2255117
ClinVar RCV Id: RCV004114376
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000648.2:p.Ala113Asp
CA301799643
NM_000657.3:c.338C>A