Canonical Allele Identifier: PA2828008819
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Thr1354Ala
CA009444
NM_001354902.2:c.4060A>G