Canonical Allele Identifier: PA2828080000
Gene: MCCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 499398
ClinVar RCV Id: RCV000595406 RCV001060906 RCV001271400
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350076.1:p.Val234Gly
CA359986148
NM_001363147.1:c.701T>G