Canonical Allele Identifier: PA2827981104
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3069608

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Arg2645Ser
CA16038748
NM_001354899.2:c.7935A>C
CA16038749
NM_001354899.2:c.7935A>T