ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826815021
Gene: CA1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000019172
ClinVar Variation:
17606
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001278896.1:p.Arg181His
CA127304
NM_001291967.2:c.542G>A