Canonical Allele Identifier: PA645436247
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 423671
ClinVar RCV Id: RCV000485098
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ala1125Gly
CA16620509
NM_032043.3:c.3374C>G