Canonical Allele Identifier: PA2828007505
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133532

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Gly1543Ala
CA009873
NM_001354905.2:c.4628G>C