Canonical Allele Identifier: PA2828051846
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1368407
ClinVar RCV Id: RCV003772579

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser231Arg
CA16023216
NM_001354905.2:c.691A>C
CA16023221
NM_001354905.2:c.693T>A
CA16023222
NM_001354905.2:c.693T>G