Canonical Allele Identifier: PA2828027711
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 958591

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ser2258Ala
CA046787
NM_001354903.2:c.6772T>G