Canonical Allele Identifier: PA2827971674
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142442

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser2571Ala
CA014059
NM_001354898.2:c.7711T>G