Canonical Allele Identifier: PA2580470784
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2107524
ClinVar RCV Id: RCV003017437
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Met299Leu
CA400484683
NM_032043.3:c.895A>T
CA400484685
NM_032043.3:c.895A>C