Canonical Allele Identifier: PA2828004279
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232691

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asn2513Lys
CA10578451
NM_001354902.2:c.7539C>G
CA16038303
NM_001354902.2:c.7539C>A