Canonical Allele Identifier: PA135078
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40364
ClinVar RCV Id: RCV000033302 RCV000037914 RCV000442182 RCV000426199 RCV001811232 RCV001813221 RCV002250499
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004324.2:p.Gly464Val
CA135076
NM_004333.6:c.1391G>T