Canonical Allele Identifier: PA2828051613
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 419482
ClinVar RCV Id: RCV000478524 RCV000573645 RCV001824796 RCV003463997 RCV004002304 RCV002496857
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Met212Ile
CA16023107
NM_001354905.2:c.636G>A
CA16023108
NM_001354905.2:c.636G>C
CA16023109
NM_001354905.2:c.636G>T