Canonical Allele Identifier: PA645436119
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 229897
ClinVar RCV Id: RCV000217097 RCV000220971 RCV000544259 RCV000989984
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Lys998Asn
CA8690414
NM_032043.3:c.2994G>C
CA400480036
NM_032043.3:c.2994G>T