Canonical Allele Identifier: PA2827962612
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 75619

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Pro2632Leu
CA16038424
NM_001354897.2:c.7895C>T