Canonical Allele Identifier: PA645402087
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser2421Leu
CA047405
NM_001127510.3:c.7262C>T