Canonical Allele Identifier: PA1139676331
Gene: CEACAM16 HGNC NCBI

Linked Data

ClinVar Variation Id: 930023
ClinVar RCV Id: RCV001195412
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001034302.2:p.Val173Ile
CA9503082
NM_001039213.4:c.517G>A