Canonical Allele Identifier: PA645432628
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 232022
ClinVar RCV Id: RCV000222811
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Thr104Ile
CA10580887
NM_032043.3:c.311C>T