Canonical Allele Identifier: PA2573175876
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 1434748
ClinVar RCV Id: RCV001984709
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014975.1:p.Val177Leu
CA343977184
NM_001014975.3:c.529G>C
CA343977185
NM_001014975.3:c.529G>T