Canonical Allele Identifier: PA2828027273
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1417078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Pro2041Ser
CA046567
NM_001354906.2:c.6121C>T