Canonical Allele Identifier: PA2827998233
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 659672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Pro2310Leu
CA16036808
NM_001354901.2:c.6929C>T