Canonical Allele Identifier: PA2827954340
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1026480
ClinVar RCV Id: RCV002242294

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Gly42Ala
CA360612059
NM_001354897.2:c.125G>C