Canonical Allele Identifier: PA105085
Gene: FAM20C HGNC NCBI
ClinVar RCV:
RCV000001082
ClinVar Variation:
1027
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064608.2:p.Gly379Glu
CA250015
NM_020223.4:c.1136G>A