Canonical Allele Identifier: PA2828046939
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3231149
ClinVar RCV Id: RCV004525220

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser2242Phe
CA046940
NM_001354904.2:c.6725C>T