Canonical Allele Identifier: PA2573287674
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1368493
ClinVar RCV Id: RCV001894663

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asn1057Asp
CA400479461
NM_032043.3:c.3169A>G