Canonical Allele Identifier: PA913199224
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 630231
ClinVar RCV Id: RCV000775408 RCV001339492 RCV004527776
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Thr1072Ala
CA8690386
NM_032043.3:c.3214A>G