Canonical Allele Identifier: PA2825637534
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411556

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Arg241Trp
CA049073
NM_001127511.3:c.721C>T