Canonical Allele Identifier: PA2827970835
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_001341827.1:p.Leu2317Phe
CA046700
NM_001354898.2:c.6951A>C
CA16036647
NM_001354898.2:c.6951A>T