Canonical Allele Identifier: PA645433774
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 407822
ClinVar RCV Id: RCV000468940 RCV003380573
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Gln634His
CA16615840
NM_032043.3:c.1902G>C
CA400479280
NM_032043.3:c.1902G>T