Canonical Allele Identifier: PA2827981106
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2677427
ClinVar RCV Id: RCV003471648

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2646Phe
CA16038755
NM_001354899.2:c.7937C>T