Canonical Allele Identifier: PA2741995012
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2937941
ClinVar RCV Id: RCV003796763
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Phe108Leu
CA400485369
NM_032043.3:c.324C>G
CA400485370
NM_032043.3:c.324C>A
CA400485375
NM_032043.3:c.322T>C