Canonical Allele Identifier: PA2828002741
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489463
ClinVar RCV Id: RCV000579477

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Arg1604Ser
CA16032447
NM_001354902.2:c.4812A>C
CA16032448
NM_001354902.2:c.4812A>T