Canonical Allele Identifier: PA2830079499
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3228126
ClinVar RCV Id: RCV004519836

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Tyr1131Ser
CA400478830
NM_032043.3:c.3392A>C