Canonical Allele Identifier: PA913199067
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 634793
ClinVar RCV Id: RCV000785562
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Gln793His
CA400482520
NM_032043.3:c.2379G>T
CA400482521
NM_032043.3:c.2379G>C