Canonical Allele Identifier: PA2827961696
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470074
ClinVar RCV Id: RCV000568988 RCV000677748 RCV002526319 RCV002307541
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Leu2352Phe
CA046700
NM_001354897.2:c.7056A>C
CA16036647
NM_001354897.2:c.7056A>T