Canonical Allele Identifier: PA2827978006
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 627841

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Met1704Leu
CA16032681
NM_001354899.2:c.5110A>C
CA16032682
NM_001354899.2:c.5110A>T