Canonical Allele Identifier: PA2827976554
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133519

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Thr1264Met
CA008722
NM_001354899.2:c.3791C>T