Canonical Allele Identifier: PA2828777962
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40384
ClinVar RCV Id: RCV000033328 RCV000677114 RCV000824924 RCV001265848 RCV003539765
ClinVar Variation Id: 180788
ClinVar RCV Id: RCV000157823
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365400.1:p.His537Gln
CA281986
NM_001378471.1:c.1611C>G
CA295914
NM_001378471.1:c.1611C>A