Canonical Allele Identifier: PA2826970510
Gene: SFTPC HGNC NCBI

Linked Data

ClinVar Variation Id: 1740774
ClinVar RCV Id: RCV002328425
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304708.1:p.Ser96Ala
CA370538212
NM_001317779.2:c.286T>G