Canonical Allele Identifier: PA2827983276
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 568451

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser511Cys
CA16024927
NM_001354900.2:c.1532C>G