Canonical Allele Identifier: PA2828002695
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 630006
ClinVar RCV Id: RCV000774872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Gly1583Ala
CA16032318
NM_001354902.2:c.4748G>C