Canonical Allele Identifier: PA645436243
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 418644
ClinVar RCV Id: RCV000478257 RCV000679784 RCV000811671 RCV001020106 RCV003463980
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Thr1123Ala
CA8690368
NM_032043.3:c.3367A>G