Canonical Allele Identifier: PA916009150
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 556402
ClinVar RCV Id: RCV000672403
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Met266Ile
CA404319004
NM_013976.3:c.798G>T
CA404319006
NM_013976.3:c.798G>A
CA404319007
NM_013976.3:c.798G>C