Canonical Allele Identifier: PA916064329
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 823457
ClinVar RCV Id: RCV001019716 RCV001873320
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ala1098Ser
CA292267341
NM_032043.3:c.3292G>T