Canonical Allele Identifier: PA2827957001
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428176
ClinVar RCV Id: RCV000491333 RCV000779717 RCV001539766 RCV003230267 RCV003743758
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Leu932Phe
CA033363
NM_001354897.2:c.2794C>T