Canonical Allele Identifier: PA2827955230
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1368407
ClinVar RCV Id: RCV003772579

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser300Arg
CA16023216
NM_001354897.2:c.898A>C
CA16023221
NM_001354897.2:c.900T>A
CA16023222
NM_001354897.2:c.900T>G