Canonical Allele Identifier: PA2827956904
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232811

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Met901Thr
CA10578343
NM_001354897.2:c.2702T>C