Canonical Allele Identifier: PA2827057020
Gene: SFTPA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3160953
ClinVar RCV Id: RCV004455839
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307743.1:p.Ala134Val
CA377353386
NM_001320814.1:c.401C>T