Allele Registry

Canonical Allele Identifier: PA177971

Gene: SFTPD HGNC NCBI

ClinVar RCV:

RCV000151865

RCV001689698

ClinVar Variation:

165219

HGVS (amino-acid)	Matching Registered Transcripts
NP_003010.4:p.Met31Thr	CA177970 NM_003019.5:c.92T>C