Canonical Allele Identifier: PA2828016153
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1041944
ClinVar RCV Id: RCV003770958
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Leu447Phe
CA16024899
NM_001354903.2:c.1341G>C
CA16024900
NM_001354903.2:c.1341G>T