Canonical Allele Identifier: PA2827980520
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133522

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2469Leu
CA013717
NM_001354899.2:c.7406C>T