Canonical Allele Identifier: PA2828023441
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133532

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Gly1602Ala
CA009873
NM_001354903.2:c.4805G>C