Canonical Allele Identifier: PA298933
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 182371
ClinVar RCV Id: RCV000160363 RCV000212299 RCV000409265 RCV000410368 RCV000205266 RCV003315958
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Thr124Ala
CA298931
NM_032043.3:c.370A>G