Canonical Allele Identifier: PA2827955237
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1764696
ClinVar RCV Id: RCV002373690

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser303Arg
CA16023234
NM_001354897.2:c.907A>C
CA16023240
NM_001354897.2:c.909T>A
CA16023241
NM_001354897.2:c.909T>G