Canonical Allele Identifier: PA2829037485
Gene: SFTPC HGNC NCBI

Linked Data

ClinVar Variation Id: 2904024
ClinVar RCV Id: RCV003727013
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372589.1:p.Gly137Ser
CA173484067
NM_001385660.1:c.409G>A