Canonical Allele Identifier: PA2580504327
Gene: C20orf144 HGNC NCBI
ClinVar RCV:
RCV004110968
ClinVar Variation:
2258224
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_543015.1:p.Arg147Gly
CA408641744
NM_080825.4:c.439C>G