Canonical Allele Identifier: PA916041579
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470111
ClinVar RCV Id: RCV001026842 RCV003537087 RCV003999435
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Gln2623His
CA16038310
NM_001354896.2:c.7869A>C
CA16038311
NM_001354896.2:c.7869A>T