Canonical Allele Identifier: PA2828628386
Gene: FAM114A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 92026
ClinVar RCV Id: RCV000122583
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362721.1:p.Gly235Ala
CA232376
NM_001375792.1:c.704G>C