Canonical Allele Identifier: PA2828012372
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489496
ClinVar RCV Id: RCV000580381

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser2490Thr
CA16038144
NM_001354902.2:c.7469G>C