Canonical Allele Identifier: PA2827940706
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135682

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Arg401Ser
CA004084
NM_001354895.2:c.1203G>T
CA16023939
NM_001354895.2:c.1203G>C