Canonical Allele Identifier: PA658724458
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 491467
ClinVar RCV Id: RCV000584290 RCV001065231
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Glu1104Asp
CA400479003
NM_032043.3:c.3312A>T
CA400479004
NM_032043.3:c.3312A>C