Allele Registry

Canonical Allele Identifier: PA2826970613

Gene: SFTPC HGNC NCBI

ClinVar RCV:

RCV000014096

RCV000261074

RCV002054436

RCV002336082

RCV003904835

ClinVar Variation:

13209

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304709.1:p.Arg161Gln	CA210538 NM_001317780.2:c.482G>A