Canonical Allele Identifier: PA2827977063
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Thr1417Ala
CA009444
NM_001354899.2:c.4249A>G