Canonical Allele Identifier: PA2828776702
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13981
ClinVar RCV Id: RCV000015015 RCV000033337 RCV000622900 RCV000763164 RCV001851863
ClinVar Variation Id: 162797
ClinVar RCV Id: RCV000150199 RCV000157831 RCV000624589 RCV000689333 RCV000767527 RCV000999624
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365398.1:p.Asp616Glu
CA279981
NM_001378469.1:c.1848T>A
CA280051
NM_001378469.1:c.1848T>G