Canonical Allele Identifier: PA2826272789
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_001191339.2:p.Pro34Ala
CA081098
NM_001204410.2:c.100C>G