Canonical Allele Identifier: PA2825021636
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1374809
ClinVar RCV Id: RCV003745371
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Lys1768Asn
CA16032926
NM_000038.6:c.5304G>C
CA16032927
NM_000038.6:c.5304G>T