Canonical Allele Identifier: PA1139741450
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 958591

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser2377Ala
CA046787
NM_001354896.2:c.7129T>G