Allele Registry

Canonical Allele Identifier: PA2825205599

Gene: SFTPB HGNC NCBI

ClinVar Variation Id: 337309

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