Canonical Allele Identifier: PA2828004267
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 161205
ClinVar RCV Id: RCV000148361 RCV000215340 RCV000458485 RCV000483957 RCV001199001 RCV003998166
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asn2502Ser
CA014033
NM_001354902.2:c.7505A>G