Canonical Allele Identifier: PA645436235
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 234243
ClinVar RCV Id: RCV000221951 RCV000477261 RCV001284123
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asp1112Glu
CA10580777
NM_032043.3:c.3336T>A
CA400478954
NM_032043.3:c.3336T>G