Canonical Allele Identifier: PA658665843
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 483144
ClinVar RCV Id: RCV000569917 RCV000586091 RCV000662391 RCV001124865 RCV001069949 RCV003316743
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asn370Ser
CA8690802
NM_032043.3:c.1109A>G