Canonical Allele Identifier: PA2828776547
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13975
ClinVar RCV Id: RCV000015009 RCV000208764 RCV000211749 RCV000680805 RCV001172276 RCV001849264 RCV003415705 RCV004018629
ClinVar Variation Id: 177844
ClinVar RCV Id: RCV000154481 RCV000844617 RCV000824921 RCV001192586 RCV003317101
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365398.1:p.Leu463Phe
CA273414
NM_001378469.1:c.1389G>C
CA280060
NM_001378469.1:c.1389G>T