ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2829037121
Gene: SFTPC
HGNC
NCBI
Linked Data
ClinVar Variation Id:
3160964
ClinVar RCV Id:
RCV004455850
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001372583.1:p.Ala164Thr
CA4664065
NM_001385654.1:c.490G>A