Canonical Allele Identifier: PA916064580
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 823817
ClinVar RCV Id: RCV001020394 RCV001873331
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ala1159Ser
CA8690359
NM_032043.3:c.3475G>T