Canonical Allele Identifier: PA2828776013
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 375940
ClinVar RCV Id: RCV000440177

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365397.1:p.Val600Arg
CA16021333
NM_001378468.1:c.1798_1799delinsAG
CA645544098
NM_001378468.1:c.1798_1799delinsCG
CA645544099
NM_001378468.1:c.1797_1799delinsGAG