Canonical Allele Identifier: PA2827976617
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231488

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ile1283Ser
CA10578361
NM_001354899.2:c.3848T>G