Canonical Allele Identifier: PA196417
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 186989
ClinVar RCV Id: RCV000166662 RCV000198324 RCV000219026 RCV000662435 RCV000781167 RCV001798598 RCV003316056
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ile1191Val
CA196415
NM_032043.3:c.3571A>G