Canonical Allele Identifier: PA658826409
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 556402
ClinVar RCV Id: RCV000672403

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Met266Ile
CA404319004
NM_000159.4:c.798G>T
CA404319006
NM_000159.4:c.798G>A
CA404319007
NM_000159.4:c.798G>C