Canonical Allele Identifier: PA157709
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 133757
ClinVar RCV Id: RCV000120401 RCV000213879 RCV000468023 RCV000656815 RCV000662595 RCV003144130 RCV003149827 RCV003315737
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Val935Gly
CA157707
NM_032043.3:c.2804T>G