Canonical Allele Identifier: PA2825644239
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 371793

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser2450Ala
CA047997
NM_001127511.3:c.7348T>G