Canonical Allele Identifier: PA2827983481
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 421285

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Thr585Ala
CA029787
NM_001354900.2:c.1753A>G