Allele Registry

Canonical Allele Identifier: PA2828778477

Gene: BRAF HGNC NCBI

ClinVar RCV:

RCV000421677

ClinVar Variation:

376072

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365401.1:p.Gly417Ser	CA16602534 NM_001378472.1:c.1249_1250delinsTC CA168090454 NM_001378472.1:c.1249_1251delinsAGT CA168090462 NM_001378472.1:c.1249_1251delinsAGC