Canonical Allele Identifier: PA2827960847
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470038

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Pro2096Ala
CA044235
NM_001354897.2:c.6286C>G