Canonical Allele Identifier: PA298849
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 182337
ClinVar RCV Id: RCV000160327 RCV000226626 RCV000573454 RCV000662546 RCV000989974 RCV003492648 RCV001192971 RCV004544466
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ala1187Thr
CA298847
NM_032043.3:c.3559G>A