Canonical Allele Identifier: PA177934
Gene: SFTPA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 165201
ClinVar RCV Id: RCV000151847
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005402.3:p.Pro193Ser
CA177933
NM_005411.5:c.577C>T