Canonical Allele Identifier: PA096804
Gene: CHST14 HGNC NCBI

Linked Data

ClinVar Variation Id: 2340
ClinVar RCV Id: RCV000002430 RCV001290019
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_569735.1:p.Pro281Leu
CA281526
NM_130468.4:c.842C>T