Canonical Allele Identifier: PA117040
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 4736
ClinVar RCV Id: RCV000005002 RCV000116124 RCV000199377 RCV000200979 RCV000410864 RCV000409748 RCV000587908 RCV000778130 RCV000990044 RCV001090025 RCV003149563
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Pro47Ala
CA117038
NM_032043.3:c.139C>G