Canonical Allele Identifier: PA2828012968
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 629231
ClinVar RCV Id: RCV000773930

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Gln2440His
CA16038272
NM_001354905.2:c.7320A>C
CA16038273
NM_001354905.2:c.7320A>T