Canonical Allele Identifier: PA2827960552
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489474

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Pro2002Ser
CA043556
NM_001354897.2:c.6004C>T