Canonical Allele Identifier: PA2580472155
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1941898
ClinVar RCV Id: RCV002643366
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Tyr1137Cys
CA400478789
NM_032043.3:c.3410A>G
CA2580094558
NM_032043.3:c.3410_3411delinsGC