Canonical Allele Identifier: PA2825968097
Gene: CHAMP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 432878
ClinVar RCV Id: RCV000498305
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157617.1:p.Pro265Ser
CA388847146
NM_001164145.3:c.793C>T