Canonical Allele Identifier: PA2827947521
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133522

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ser2497Leu
CA013717
NM_001354895.2:c.7490C>T