Canonical Allele Identifier: PA2828029139
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 629231
ClinVar RCV Id: RCV000773930

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Gln2317His
CA16038272
NM_001354906.2:c.6951A>C
CA16038273
NM_001354906.2:c.6951A>T