Canonical Allele Identifier: PA2825023940
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 958591

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser2359Ala
CA046787
NM_000038.6:c.7075T>G