Canonical Allele Identifier: PA645436218
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 407875
ClinVar RCV Id: RCV000463699 RCV000573765 RCV001567368
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ile1103Asn
CA16615762
NM_032043.3:c.3308T>A