Canonical Allele Identifier: PA169465
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 142809
ClinVar RCV Id: RCV000132232 RCV000213770 RCV000687515 RCV000990039 RCV004532579 RCV002267884
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asn109Ser
CA169463
NM_032043.3:c.326A>G