Canonical Allele Identifier: PA916040243
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41530

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Pro1476Ser
CA009490
NM_001354896.2:c.4426C>T