Canonical Allele Identifier: PA2825024171
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser2421Leu
CA047405
NM_000038.6:c.7262C>T