Canonical Allele Identifier: PA167684
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 142179
ClinVar RCV Id: RCV000131157 RCV000231925 RCV000220964 RCV000412159 RCV000411077 RCV000781177 RCV001356435 RCV002225442 RCV003315902
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.His285Arg
CA167682
NM_032043.3:c.854A>G