Canonical Allele Identifier: PA2825014994
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2822243
ClinVar RCV Id: RCV003650976

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Cys447Ser
CA16024236
NM_000038.6:c.1339T>A
CA16024240
NM_000038.6:c.1340G>C