Canonical Allele Identifier: PA2828026004
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470038

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Pro1985Ala
CA044235
NM_001354903.2:c.5953C>G