Canonical Allele Identifier: PA2827946850
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 644645

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ser2295Ala
CA16036352
NM_001354895.2:c.6883T>G