Canonical Allele Identifier: PA356739
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 219645
ClinVar RCV Id: RCV000204761 RCV000221756 RCV000320950 RCV001192827 RCV001575907
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Phe934Ser
CA348966
NM_032043.3:c.2801T>C