Canonical Allele Identifier: PA2825021422
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asn1716Ser
CA040767
NM_000038.6:c.5147A>G