Canonical Allele Identifier: PA2828229840
Gene: SFTPB HGNC NCBI

Linked Data

ClinVar Variation Id: 1766887
ClinVar RCV Id: RCV002373973
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354210.1:p.Cys302Gly
CA347487352
NM_001367281.1:c.904T>G