Canonical Allele Identifier: PA104961
Gene: MCCC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064551.3:p.Met325Arg
CA251975
NM_020166.5:c.974T>G