Canonical Allele Identifier: PA2827971753
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411484

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Pro2597Ala
CA16038420
NM_001354898.2:c.7789C>G