Canonical Allele Identifier: PA2827967444
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231488

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ile1286Ser
CA10578361
NM_001354898.2:c.3857T>G