Canonical Allele Identifier: PA916050579
Gene: FAM53C HGNC NCBI

Linked Data

ClinVar Variation Id: 91932
ClinVar RCV Id: RCV000122490
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057689.1:p.Pro164Ser
CA232188
NM_016605.3:c.490C>T