Canonical Allele Identifier: PA2827980086
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232940
ClinVar RCV Id: RCV000220467 RCV000236554 RCV001280597 RCV002291603 RCV002478806 RCV003650501 RCV003998013
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Pro2341Ser
CA046951
NM_001354899.2:c.7021C>T