Canonical Allele Identifier: PA2825634852
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_001120982.1:p.Met2364Leu
CA16036773
NM_001127510.3:c.7090A>C
CA16036774
NM_001127510.3:c.7090A>T