Canonical Allele Identifier: PA2828779349
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 422080
ClinVar RCV Id: RCV000486116

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365402.1:p.Ile703Ser
CA16618359
NM_001378473.1:c.2108_2109delinsGT
CA369537050
NM_001378473.1:c.2108T>G