Canonical Allele Identifier: PA645432976
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 279708
ClinVar RCV Id: RCV000319358 RCV000573698 RCV000636175
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asn293Ser
CA8690839
NM_032043.3:c.878A>G