Allele Registry

Canonical Allele Identifier: PA2825205609

Gene: SFTPB HGNC NCBI

ClinVar RCV:

RCV000014091

RCV001778652

RCV002381249

ClinVar Variation:

13204

HGVS (amino-acid)	Matching Registered Transcripts
NP_000533.4:p.Arg236Cys	CA210533 NM_000542.5:c.706C>T