Canonical Allele Identifier: PA356748
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 219482

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ser1076Leu
CA349030
NM_032043.3:c.3227C>T