Canonical Allele Identifier: PA2827973840
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 937461

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Gln417His
CA16024227
NM_001354899.2:c.1251G>C
CA16024228
NM_001354899.2:c.1251G>T