Canonical Allele Identifier: PA2580162888
Gene: SEC14L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2207579
ClinVar RCV Id: RCV004074230
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137473.2:p.Asn70Ser
CA8792257
NM_001144001.2:c.209A>G