Canonical Allele Identifier: PA645436156
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 241650
ClinVar RCV Id: RCV000233906 RCV000989983 RCV001175823
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Met1041Thr
CA8690394
NM_032043.3:c.3122T>C