Canonical Allele Identifier: PA916040392
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142201
ClinVar RCV Id: RCV000131191 RCV000232313 RCV000211915 RCV001157157 RCV001818321 RCV003315903 RCV003492615 RCV003998088 RCV003325188
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Arg1607Gly
CA009730
NM_001354896.2:c.4819C>G