Canonical Allele Identifier: PA916062482
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 663682
ClinVar RCV Id: RCV000821608 RCV001011020
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Cys442Arg
CA400483383
NM_032043.3:c.1324T>C