Canonical Allele Identifier: PA2829037486
Gene: SFTPC HGNC NCBI

Linked Data

ClinVar Variation Id: 1389667
ClinVar RCV Id: RCV001898005
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372589.1:p.Glu138Lys
CA4664081
NM_001385660.1:c.412G>A