Canonical Allele Identifier: PA2828775860
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 376072
ClinVar RCV Id: RCV000421677
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365397.1:p.Gly469Ser
CA16602534
NM_001378468.1:c.1405_1406delinsTC
CA168090454
NM_001378468.1:c.1405_1407delinsAGT
CA168090462
NM_001378468.1:c.1405_1407delinsAGC