Canonical Allele Identifier: PA2580472230
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1733227
ClinVar RCV Id: RCV002455340
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ser1204Arg
CA292267138
NM_032043.3:c.3612T>A
CA400478035
NM_032043.3:c.3612T>G
CA400478044
NM_032043.3:c.3610A>C