Canonical Allele Identifier: PA645402028
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231537
ClinVar RCV Id: RCV003534521 RCV000218412
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Gln2376His
CA047019
NM_001127510.3:c.7128G>C
CA16036857
NM_001127510.3:c.7128G>T