Canonical Allele Identifier: PA2828041890
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1051201

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asn1524Ser
CA040262
NM_001354904.2:c.4571A>G