ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826970466
Gene: SFTPC
HGNC
NCBI
Linked Data
ClinVar Variation Id:
13214
ClinVar RCV Id:
RCV000014101
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001304707.1:p.Leu188Pro
CA210546
NM_001317778.2:c.563T>C