Canonical Allele Identifier: PA156807
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133522

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser2497Leu
CA013717
NM_000038.6:c.7490C>T