ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826063344
Gene: SFTPC
HGNC
NCBI
Linked Data
ClinVar Variation Id:
362560
ClinVar RCV Id:
RCV000305466
RCV000391181
RCV001358404
RCV002248630
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001165828.1:p.Ala149Pro
CA4664059
NM_001172357.2:c.445G>C