Canonical Allele Identifier: PA2741863554
Gene: SFTPA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3027274
ClinVar RCV Id: RCV003887667
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307743.1:p.Tyr250del
CA2740093041
NM_001320814.1:c.749_751del