Canonical Allele Identifier: PA2828049117
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3069608

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Arg2547Ser
CA16038748
NM_001354904.2:c.7641A>C
CA16038749
NM_001354904.2:c.7641A>T