Canonical Allele Identifier: PA2828023079
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1051201

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Asn1549Ser
CA040262
NM_001354903.2:c.4646A>G