Canonical Allele Identifier: PA645432690
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 232380
ClinVar RCV Id: RCV000216740 RCV000705215 RCV001800562
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Thr121Ser
CA8690958
NM_032043.3:c.362C>G
CA400485297
NM_032043.3:c.361A>T