Canonical Allele Identifier: PA916064562
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 658027
ClinVar RCV Id: RCV000814760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asp1153Gly
CA400478682
NM_032043.3:c.3458A>G