Canonical Allele Identifier: PA2827963311
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470146

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Pro2841Leu
CA050906
NM_001354897.2:c.8522C>T