Canonical Allele Identifier: PA2825021152
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1051201

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asn1650Ser
CA040262
NM_000038.6:c.4949A>G