Canonical Allele Identifier: PA2827958722
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 230719

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Lys1447Arg
CA038588
NM_001354897.2:c.4340A>G