Canonical Allele Identifier: PA2825533253
Gene: SFTPA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2390476
ClinVar RCV Id: RCV002694209
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092138.1:p.Val134Ala
CA5574042
NM_001098668.2:c.401T>C