Canonical Allele Identifier: PA2828012426
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231400

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asn2350Ser
CA10578446
NM_001354905.2:c.7049A>G