Canonical Allele Identifier: PA2828042936
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2015366
ClinVar RCV Id: RCV003742952
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Thr1647Ser
CA16032959
NM_001354904.2:c.4939A>T
CA16032961
NM_001354904.2:c.4940C>G