Canonical Allele Identifier: PA2827983260
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2748653
ClinVar RCV Id: RCV003536633

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser505Gly
CA16024881
NM_001354900.2:c.1513A>G
CA2697546184
NM_001354900.2:c.1512_1513delinsAG