Canonical Allele Identifier: PA2827964701
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490193

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ala424Val
CA16024253
NM_001354898.2:c.1271C>T