Canonical Allele Identifier: PA916070948
Gene: SPPL2C HGNC NCBI
ClinVar RCV:
RCV000969825
ClinVar Variation:
787567
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_787078.2:p.Tyr46Cys
CA8617023
NM_175882.3:c.137A>G