Canonical Allele Identifier: PA2580472169
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1731587
ClinVar RCV Id: RCV002337461
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Thr1152Ser
CA400478688
NM_032043.3:c.3455C>G
CA400478690
NM_032043.3:c.3454A>T