Canonical Allele Identifier: PA2829605422
Gene: SFTPA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 229244
ClinVar RCV Id: RCV000217793
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005402.3:p.Asp45Glu
CA5574393
NM_005411.5:c.135C>G
CA5574394
NM_005411.5:c.135C>A