Canonical Allele Identifier: PA2826970619
Gene: SFTPC HGNC NCBI

Linked Data

ClinVar Variation Id: 1708000
ClinVar RCV Id: RCV002287161
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304709.1:p.Gly176Asp
CA370538405
NM_001317780.2:c.527G>A