Allele Registry

Canonical Allele Identifier: PA916061205

Gene: SFTPB HGNC NCBI

ClinVar RCV:

RCV000014091

RCV001778652

RCV002381249

ClinVar Variation:

13204

HGVS (amino-acid)	Matching Registered Transcripts
NP_942140.3:p.Arg236Cys	CA210533 NM_198843.3:c.706C>T