Canonical Allele Identifier: PA2825021087
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482266

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Pro1634Leu
CA040139
NM_000038.6:c.4901C>T