Canonical Allele Identifier: PA2828000274
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418008

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ala349Thr
CA16024191
NM_001354902.2:c.1045G>A