Canonical Allele Identifier: PA2825024470
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 487060

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser2497Trp
CA16037624
NM_000038.6:c.7490C>G