Canonical Allele Identifier: PA2826272752
Gene: SEC14L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2207579
ClinVar RCV Id: RCV004074230
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191337.2:p.Asn104Ser
CA8792257
NM_001204408.2:c.311A>G