Canonical Allele Identifier: PA645400049
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 230719

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Lys1437Arg
CA038588
NM_001127510.3:c.4310A>G