Canonical Allele Identifier: PA645497653
Gene: ALG14 HGNC NCBI

Linked Data

ClinVar Variation Id: 376840
ClinVar RCV Id: RCV000432703 RCV000503682 RCV001257053 RCV002480277 RCV003343807 RCV003343806 RCV003932543
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659425.1:p.Ala11Thr
CA961908
NM_144988.4:c.31G>A