Canonical Allele Identifier: PA916058770
Gene: CHST14 HGNC NCBI

Linked Data

ClinVar Variation Id: 656214
ClinVar RCV Id: RCV000812575
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_569735.1:p.Pro26Leu
CA391762099
NM_130468.4:c.77C>T