Canonical Allele Identifier: PA645436240
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 407862
ClinVar RCV Id: RCV000466152 RCV003153616
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asn1118Ser
CA16615470
NM_032043.3:c.3353A>G