Canonical Allele Identifier: PA2825643031
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489476

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asp2061Ala
CA044147
NM_001127511.3:c.6182A>C