Canonical Allele Identifier: PA2827995679
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231392

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Lys1527Met
CA039747
NM_001354901.2:c.4580A>T