Canonical Allele Identifier: PA2827985077
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser1087Cys
CA035180
NM_001354900.2:c.3260C>G