Canonical Allele Identifier: PA2827946138
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489476

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Asp2079Ala
CA044147
NM_001354895.2:c.6236A>C