Canonical Allele Identifier: PA2827999038
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 433677

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Arg2554Lys
CA16038358
NM_001354901.2:c.7661G>A