Canonical Allele Identifier: PA645436181
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 324347
ClinVar RCV Id: RCV000364269 RCV000775231
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Thr1084Ser
CA10649748
NM_032043.3:c.3251C>G
CA400479128
NM_032043.3:c.3250A>T