Canonical Allele Identifier: PA645436163
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 241652
ClinVar RCV Id: RCV000231423 RCV001798742 RCV003165648
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Cys1067Ser
CA10583614
NM_032043.3:c.3199T>A
CA400479341
NM_032043.3:c.3200G>C