Canonical Allele Identifier: PA2827959619
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469991
ClinVar RCV Id: RCV001189874 RCV001775866 RCV003742727
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Thr1719Ser
CA16032532
NM_001354897.2:c.5155A>T
CA16032534
NM_001354897.2:c.5156C>G