Canonical Allele Identifier: PA916064531
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 823747
ClinVar RCV Id: RCV001020242 RCV001873330
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Pro1139Ser
CA400478778
NM_032043.3:c.3415C>T