Canonical Allele Identifier: PA2827970846
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41512

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Pro2321Ser
CA012759
NM_001354898.2:c.6961C>T