Canonical Allele Identifier: PA2828008920
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490277
ClinVar RCV Id: RCV000581992 RCV003153754 RCV003653203
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Thr1405Ser
CA039198
NM_001354902.2:c.4214C>G
CA16031154
NM_001354902.2:c.4213A>T