Canonical Allele Identifier: PA645479895
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 235858
ClinVar RCV Id: RCV000224360
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Gln144Pro
CA10581470
NM_000159.4:c.431A>C