Canonical Allele Identifier: PA288572
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 128180
ClinVar RCV Id: RCV000116149 RCV000409338 RCV000585934 RCV000411198 RCV000199089 RCV001030467 RCV000855583 RCV003315655 RCV004529951 RCV003492507
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Gln944Glu
CA288570
NM_032043.3:c.2830C>G