Allele Registry

Canonical Allele Identifier: PA177965

Gene: SFTPD HGNC NCBI

ClinVar RCV:

RCV000151861

RCV001651021

ClinVar Variation:

165215

HGVS (amino-acid)	Matching Registered Transcripts
NP_003010.4:p.Thr180Ala	CA177964 NM_003019.5:c.538A>G