Canonical Allele Identifier: PA157697
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 133753
ClinVar RCV Id: RCV000120397 RCV000165749 RCV000475545 RCV000656813 RCV000663063 RCV001030536 RCV003153386 RCV003315735 RCV003492523
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asn775Ser
CA157695
NM_032043.3:c.2324A>G