Canonical Allele Identifier: PA645433749
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 419768
ClinVar RCV Id: RCV000487183 RCV000554110 RCV001013389 RCV001821394
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Leu617Ser
CA16620528
NM_032043.3:c.1850T>C