Canonical Allele Identifier: PA2825070013
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 2736816
ClinVar RCV Id: RCV003497352
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Asp220Tyr
CA404318517
NM_000159.4:c.658G>T