Canonical Allele Identifier: PA2827960063
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470012

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Pro1853Thr
CA16033423
NM_001354897.2:c.5557C>A