Canonical Allele Identifier: PA2828229817
Gene: SFTPB HGNC NCBI

Linked Data

ClinVar Variation Id: 13204
ClinVar RCV Id: RCV000014091 RCV001778652 RCV002381249
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354210.1:p.Arg236Cys
CA210533
NM_001367281.1:c.706C>T