Canonical Allele Identifier: PA2827962664
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 350423

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Thr2645Ala
CA10622269
NM_001354897.2:c.7933A>G