Canonical Allele Identifier: PA2825644643
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 629231
ClinVar RCV Id: RCV000773930

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Gln2582His
CA16038272
NM_001127511.3:c.7746A>C
CA16038273
NM_001127511.3:c.7746A>T