Canonical Allele Identifier: PA288608
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 128194
ClinVar RCV Id: RCV000116163 RCV000235147 RCV000586611 RCV001030546 RCV001127949 RCV001356235 RCV001082539 RCV001356416 RCV003149814 RCV004529954
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asn196Ser
CA288606
NM_032043.3:c.587A>G