Canonical Allele Identifier: PA2741995224
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2564578
ClinVar RCV Id: RCV003297010

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asn1057Ser
CA292267466
NM_032043.3:c.3170A>G