Allele Registry

Canonical Allele Identifier: PA645490308

Gene: SFTPC HGNC NCBI

ClinVar RCV:

RCV000271807

RCV000366166

RCV002248629

RCV002402077

RCV002509375

RCV003556368

ClinVar Variation:

362554

HGVS (amino-acid)	Matching Registered Transcripts
NP_003009.2:p.His59Arg	CA4663918 NM_003018.4:c.176A>G