Allele Registry

Canonical Allele Identifier: PA2826970618

Gene: SFTPC HGNC NCBI

ClinVar RCV:

RCV000262185

RCV000331564

RCV001431879

RCV002348113

ClinVar Variation:

362562

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304709.1:p.Leu175Val	CA4664075 NM_001317780.2:c.523C>G