Canonical Allele Identifier: PA658663689
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 448994
ClinVar RCV Id: RCV000522943 RCV000553783 RCV000775412
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ala939Gly
CA8690454
NM_032043.3:c.2816C>G