Canonical Allele Identifier: PA916064377
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 823568
ClinVar RCV Id: RCV001019926 RCV001873323
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Leu1105Phe
CA400478996
NM_032043.3:c.3315G>T
CA400478997
NM_032043.3:c.3315G>C