Canonical Allele Identifier: PA2827995204
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Thr1386Ala
CA009444
NM_001354901.2:c.4156A>G