Canonical Allele Identifier: PA2573098378
Gene: CHST14 HGNC NCBI

Linked Data

ClinVar Variation Id: 1310688
ClinVar RCV Id: RCV001767802 RCV003298972
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_569735.1:p.Ala373Val
CA7481700
NM_130468.4:c.1118C>T