Canonical Allele Identifier: PA2828002332
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186645
ClinVar RCV Id: RCV000166273 RCV000236286 RCV001155477 RCV001704215 RCV003765040 RCV003995494
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asp1421Asn
CA009616
NM_001354902.2:c.4261G>A