Canonical Allele Identifier: PA2826970625
Gene: SFTPC HGNC NCBI

Linked Data

ClinVar Variation Id: 2735140
ClinVar RCV Id: RCV003557385
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304709.1:p.Cys183Gly
CA370538444
NM_001317780.2:c.547T>G