Canonical Allele Identifier: PA2828004025
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537519
ClinVar RCV Id: RCV003538489
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Gln2349His
CA16037271
NM_001354902.2:c.7047G>C
CA16037272
NM_001354902.2:c.7047G>T