Canonical Allele Identifier: PA2825862459
Gene: SEC14L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 222961
ClinVar RCV Id: RCV000208543
JSON-LD

Amino-acid Alleles

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