Canonical Allele Identifier: PA2827976121
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Thr1132Ala
CA035507
NM_001354899.2:c.3394A>G