Canonical Allele Identifier: PA2830079442
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3228125
ClinVar RCV Id: RCV004519835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Thr1116Ser
CA400478927
NM_032043.3:c.3347C>G
CA400478929
NM_032043.3:c.3346A>T