Canonical Allele Identifier: PA645433242
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 407835
ClinVar RCV Id: RCV000462189 RCV000563667 RCV001124866 RCV001194724 RCV001584150 RCV003463896 RCV004533180
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Leu340Phe
CA8690816
NM_032043.3:c.1018C>T