Canonical Allele Identifier: PA2827977741
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1051201

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asn1622Ser
CA040262
NM_001354899.2:c.4865A>G