Canonical Allele Identifier: PA2827989494
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127318
ClinVar RCV Id: RCV000120031 RCV000115120 RCV000148360 RCV000590816 RCV000735966 RCV003650373 RCV001353987
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Pro2426Thr
CA013653
NM_001354900.2:c.7276C>A