Canonical Allele Identifier: PA259662
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 29805
ClinVar RCV Id: RCV000022678 RCV000033281 RCV000208540 RCV000211753 RCV000545320 RCV000515432 RCV001329218 RCV003230371 RCV003398558
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004324.2:p.Thr241Met
CA259660
NM_004333.6:c.722C>T