Canonical Allele Identifier: PA2828001991
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231488

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ile1220Ser
CA10578361
NM_001354902.2:c.3659T>G