Canonical Allele Identifier: PA645433730
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 233608
ClinVar RCV Id: RCV000218989 RCV000473133 RCV000482369 RCV000662848 RCV003316229
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.His587Asp
CA10580830
NM_032043.3:c.1759C>G