Canonical Allele Identifier: PA294092
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141191
ClinVar RCV Id: RCV000129585 RCV000167896 RCV000211912 RCV000588058 RCV003315877 RCV003997513
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ala1358Thr
CA008897
NM_000038.6:c.4072G>A