Canonical Allele Identifier: PA2827958307
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231488

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ile1321Ser
CA10578361
NM_001354897.2:c.3962T>G