Canonical Allele Identifier: PA2828013617
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 82636
ClinVar RCV Id: RCV000073625
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Met2553Leu
CA014373
NM_001354905.2:c.7657A>C
CA16039003
NM_001354905.2:c.7657A>T