Canonical Allele Identifier: PA2828027356
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 826775

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Pro2055Ser
CA046630
NM_001354906.2:c.6163C>T