Canonical Allele Identifier: PA916042492
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser968Cys
CA035180
NM_001354905.2:c.2903C>G