Canonical Allele Identifier: PA2499292696
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1044878

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Lys1078Asn
CA8690383
NM_032043.3:c.3234G>T
CA400479203
NM_032043.3:c.3234G>C