Canonical Allele Identifier: PA2827959549
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 419787

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Pro1701Thr
CA16032418
NM_001354897.2:c.5101C>A