Canonical Allele Identifier: PA334614
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 188324

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ser206Leu
CA334612
NM_032043.3:c.617C>T