Canonical Allele Identifier: PA166322
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 141761
ClinVar RCV Id: RCV000130394 RCV000200420 RCV000590600 RCV000662423 RCV001290444 RCV003315892 RCV004532557
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Pro210Ser
CA166320
NM_032043.3:c.628C>T