ClinGen Allele Registry
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Canonical Allele Identifier:
PA288569
Gene: BRIP1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
133636
ClinVar RCV:
RCV000116148
RCV000212329
RCV000229209
RCV000410789
RCV000412341
RCV000656814
RCV003315654
ClinVar Variation:
128179
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_114432.2:p.Ile902Met
CA288567
NM_032043.3:c.2706A>G