Canonical Allele Identifier: PA2499292697
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1045624
ClinVar RCV Id: RCV001350068

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Pro1101Leu
CA400479023
NM_032043.3:c.3302C>T