Canonical Allele Identifier: PA2825644617
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428129

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.His2573Asp
CA16038213
NM_001127511.3:c.7717C>G