Canonical Allele Identifier: PA2580481769
Gene: CHAMP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2280795
ClinVar RCV Id: RCV002818884
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115812.1:p.Pro406Ser
CA388848125
NM_032436.4:c.1216C>T