Canonical Allele Identifier: PA913200444
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 629231
ClinVar RCV Id: RCV000773930

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Gln2600His
CA16038272
NM_001127510.3:c.7800A>C
CA16038273
NM_001127510.3:c.7800A>T