Canonical Allele Identifier: PA2827978086
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236616

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ala1727Val
CA041104
NM_001354899.2:c.5180C>T