Canonical Allele Identifier: PA2825862459
Gene: SEC14L1 HGNC NCBI
ClinVar RCV:
RCV000208543
ClinVar Variation:
222961
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137471.2:p.Pro34Ala
CA081098
NM_001143999.2:c.100C>G