Canonical Allele Identifier: PA2828777877
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711751
ClinVar RCV Id: RCV002293296
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365400.1:p.Tyr435Ser
CA369588866
NM_001378471.1:c.1304A>C