Canonical Allele Identifier: PA2827968711
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232998

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Thr1672Ala
CA10578392
NM_001354898.2:c.5014A>G