Canonical Allele Identifier: PA913199232
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 628857
ClinVar RCV Id: RCV000773520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asn1087Asp
CA400479110
NM_032043.3:c.3259A>G