Canonical Allele Identifier: PA2741954757
Gene: C1QTNF5 HGNC NCBI

Linked Data

ClinVar Variation Id: 3009750
ClinVar RCV Id: RCV003864861
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056460.1:p.Ser107Arg
CA382969469
NM_015645.5:c.321C>G
CA382969471
NM_015645.5:c.321C>A
CA382969479
NM_015645.5:c.319A>C