Canonical Allele Identifier: PA2827956379
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ala745Val
CA007259
NM_001354897.2:c.2234C>T