Canonical Allele Identifier: PA2827948625
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470146

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Pro2831Leu
CA050906
NM_001354895.2:c.8492C>T