Canonical Allele Identifier: PA645432811
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 422627
ClinVar RCV Id: RCV000483934 RCV000565081 RCV000811860
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Pro163Ser
CA16620544
NM_032043.3:c.487C>T