Canonical Allele Identifier: PA164073
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140969
ClinVar RCV Id: RCV000129257 RCV003650389
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ile638Met
CA006359
NM_001127510.3:c.1914A>G