Canonical Allele Identifier: PA2499292629
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1036605
ClinVar RCV Id: RCV001339642
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asn1057Lys
CA400479448
NM_032043.3:c.3171T>A
CA400479450
NM_032043.3:c.3171T>G