Canonical Allele Identifier: PA2827962110
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 371793

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser2478Ala
CA047997
NM_001354897.2:c.7432T>G