Canonical Allele Identifier: PA2827979422
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470050

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Pro2142Ser
CA16035571
NM_001354899.2:c.6424C>T