Canonical Allele Identifier: PA2827971697
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232691

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asn2579Lys
CA10578451
NM_001354898.2:c.7737C>G
CA16038303
NM_001354898.2:c.7737C>A