Canonical Allele Identifier: PA2828007810
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236616

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ala1595Val
CA041104
NM_001354905.2:c.4784C>T