Canonical Allele Identifier: PA2829037198
Gene: SFTPC HGNC NCBI

Linked Data

ClinVar Variation Id: 1750349
ClinVar RCV Id: RCV002353616
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372584.1:p.Ile197Leu
CA370538493
NM_001385655.1:c.589A>C