Canonical Allele Identifier: PA2827989483
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 569210

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser2423Cys
CA16037430
NM_001354900.2:c.7268C>G