Canonical Allele Identifier: PA2827962616
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489498

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Pro2632Thr
CA16038419
NM_001354897.2:c.7894C>A