Canonical Allele Identifier: PA2827958751
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Thr1455Ala
CA009444
NM_001354897.2:c.4363A>G