Canonical Allele Identifier: PA2828002873
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236616

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ala1664Val
CA041104
NM_001354902.2:c.4991C>T