Canonical Allele Identifier: PA095637
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 198396
ClinVar RCV Id: RCV000179723 RCV000724678
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Met191Thr
CA275381
NM_000159.4:c.572T>C