Canonical Allele Identifier: PA2828007575
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asn1556Ser
CA040767
NM_001354905.2:c.4667A>G