Canonical Allele Identifier: PA916041877
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 802134
ClinVar RCV Id: RCV000987556 RCV001176396
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.His402Gln
CA16023880
NM_001354897.2:c.1206C>A
CA16023881
NM_001354897.2:c.1206C>G