Canonical Allele Identifier: PA177935
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_001087239.2:p.Pro208Ser
CA177933
NM_001093770.3:c.622C>T