Canonical Allele Identifier: PA1139729157
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 891665
ClinVar RCV Id: RCV001127095
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Leu317Phe
CA404319631
NM_013976.3:c.949C>T