Canonical Allele Identifier: PA2827987030
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asn1675Ser
CA040767
NM_001354900.2:c.5024A>G