Canonical Allele Identifier: PA2499233688
Gene: C8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1169492
ClinVar RCV Id: RCV001520827 RCV003980598
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000553.1:p.Pro34Ser
CA874915
NM_000562.3:c.100C>T