Canonical Allele Identifier: PA2741995232
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2630713
ClinVar RCV Id: RCV003778226 RCV004527917
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Thr1116Ala
CA400478930
NM_032043.3:c.3346A>G