Canonical Allele Identifier: PA2825023854
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 826775

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Pro2338Ser
CA046630
NM_000038.6:c.7012C>T