Canonical Allele Identifier: PA658676634
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 459951
ClinVar RCV Id: RCV000531618 RCV004526700
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Val133Met
CA404317460
NM_000159.4:c.397G>A