Canonical Allele Identifier: PA645432682
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 241657
ClinVar RCV Id: RCV000229479 RCV004020884
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asn119Lys
CA10583641
NM_032043.3:c.357T>A
CA400485304
NM_032043.3:c.357T>G