Canonical Allele Identifier: PA2827941428
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140969

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ile638Met
CA006359
NM_001354895.2:c.1914A>G