Allele Registry

Canonical Allele Identifier: PA2825205599

Gene: SFTPB HGNC NCBI

ClinVar Allele:

287428

ClinVar RCV:

RCV000371293

RCV002057720

RCV002356470

ClinVar Variation:

337309

HGVS (amino-acid)	Matching Registered Transcripts
NP_000533.4:p.Ala187Val	CA1744007 NM_000542.5:c.560C>T