Allele Registry

Canonical Allele Identifier: PA2826970610

Gene: SFTPC HGNC NCBI

ClinVar RCV:

RCV000305466

RCV000391181

RCV001358404

RCV002248630

ClinVar Variation:

362560

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304709.1:p.Ala149Pro	CA4664059 NM_001317780.2:c.445G>C