Canonical Allele Identifier: PA2826970526
Gene: SFTPC HGNC NCBI

Linked Data

ClinVar Variation Id: 13210
ClinVar RCV Id: RCV000014097
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304708.1:p.Leu135Gln
CA210540
NM_001317779.2:c.404T>A