Canonical Allele Identifier: PA2825021155
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 949271
ClinVar RCV Id: RCV003650743
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asn1650Tyr
CA16032166
NM_000038.6:c.4948A>T