Canonical Allele Identifier: PA2827981073
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 565362

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Pro2637Ser
CA16038695
NM_001354899.2:c.7909C>T