Canonical Allele Identifier: PA916064267
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 823289
ClinVar RCV Id: RCV001019418 RCV002550846
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Thr1082Ser
CA400479144
NM_032043.3:c.3245C>G
CA400479148
NM_032043.3:c.3244A>T