Canonical Allele Identifier: PA16039961
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 230719

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Lys1437Arg
CA038588
NM_000038.6:c.4310A>G