Canonical Allele Identifier: PA2827962572
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760781
ClinVar RCV Id: RCV002410000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Lys2619Glu
CA16038330
NM_001354897.2:c.7855A>G