Canonical Allele Identifier: PA2830079378
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3228123
ClinVar RCV Id: RCV004519833
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Glu1097Asp
CA400479044
NM_032043.3:c.3291A>C
CA400479045
NM_032043.3:c.3291A>T