Canonical Allele Identifier: PA2828012842
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489496
ClinVar RCV Id: RCV000580381

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser2421Thr
CA16038144
NM_001354905.2:c.7262G>C