Canonical Allele Identifier: PA916064392
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 823618
ClinVar RCV Id: RCV001020012
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Glu1111Asp
CA400478959
NM_032043.3:c.3333A>T
CA400478960
NM_032043.3:c.3333A>C