Canonical Allele Identifier: PA332276
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135719

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asn2542Ser
CA013956
NM_001127510.3:c.7625A>G