Canonical Allele Identifier: PA298930
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 136154
ClinVar RCV Id: RCV000123365 RCV000160362 RCV000586716 RCV001125839 RCV002225394 RCV002267867 RCV003149846
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Thr260Ala
CA298928
NM_032043.3:c.778A>G