Canonical Allele Identifier: PA156862
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133533
ClinVar RCV Id: RCV000120043 RCV000546435 RCV000574195 RCV003315719 RCV003997334 RCV001356898
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Gly2303Arg
CA012645
NM_000038.6:c.6907G>A
CA16036399
NM_000038.6:c.6907G>C