Canonical Allele Identifier: PA658663726
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 481639
ClinVar RCV Id: RCV000569183 RCV000696070
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Gly1009Glu
CA400479966
NM_032043.3:c.3026G>A