Canonical Allele Identifier: PA2827970901
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1404451
ClinVar RCV Id: RCV003772768
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Met2339Leu
CA16036773
NM_001354898.2:c.7015A>C
CA16036774
NM_001354898.2:c.7015A>T