Allele Registry

Canonical Allele Identifier: PA210537

Gene: SFTPC HGNC NCBI

ClinVar RCV:

RCV000014095

RCV000731190

RCV002415413

RCV002509156

ClinVar Variation:

13208

HGVS (amino-acid)	Matching Registered Transcripts
NP_003009.2:p.Ile73Thr	CA210536 NM_003018.4:c.218T>C