Canonical Allele Identifier: PA658663832
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 479478
ClinVar RCV Id: RCV000563144 RCV001865711
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asn1147Asp
CA400478723
NM_032043.3:c.3439A>G