Canonical Allele Identifier: PA2828040267
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41530

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Pro1332Ser
CA009490
NM_001354904.2:c.3994C>T