Canonical Allele Identifier: PA1139673542
Gene: BRCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 481604
ClinVar RCV Id: RCV000568806
ClinVar Variation Id: 954632

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000050.3:p.Phe1142Leu
CA387776533
NM_000059.4:c.3424T>C
CA387776543
NM_000059.4:c.3426T>A
CA387776545
NM_000059.4:c.3426T>G