Allele Registry

Canonical Allele Identifier: PA2828776517

Gene: BRAF HGNC NCBI

ClinVar RCV:

RCV000421677

ClinVar Variation:

376072

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365398.1:p.Gly447Ser	CA16602534 NM_001378469.1:c.1339_1340delinsTC CA168090454 NM_001378469.1:c.1339_1341delinsAGT CA168090462 NM_001378469.1:c.1339_1341delinsAGC