Canonical Allele Identifier: PA645432839
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 231272
ClinVar RCV Id: RCV000223649 RCV002518300
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Val187Phe
CA10580870
NM_032043.3:c.559G>T