Canonical Allele Identifier: PA645436141
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 230429
ClinVar RCV Id: RCV000215643 RCV000484982 RCV001087512 RCV001818520
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Glu1027Lys
CA8690401
NM_032043.3:c.3079G>A