Canonical Allele Identifier: PA2827979861
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411353
ClinVar RCV Id: RCV003766557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Pro2271Ser
CA16036378
NM_001354899.2:c.6811C>T