Canonical Allele Identifier: PA334614
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 188324
ClinVar RCV Id: RCV000168335 RCV000222015 RCV000506651 RCV000662572 RCV001546767 RCV003316070
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ser206Leu
CA334612
NM_032043.3:c.617C>T