Canonical Allele Identifier: PA2826372409
Gene: CHIT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1600219
ClinVar RCV Id: RCV002132191
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243054.2:p.Asn81Lys
CA1340034
NM_001256125.2:c.243T>G
CA344313964
NM_001256125.2:c.243T>A