Canonical Allele Identifier: PA294474
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 142732
ClinVar RCV Id: RCV000132105 RCV000470512 RCV000989989
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Lys968Glu
CA294472
NM_032043.3:c.2902A>G