Canonical Allele Identifier: PA2826970608
Gene: SFTPC HGNC NCBI

Linked Data

ClinVar Variation Id: 2500719
ClinVar RCV Id: RCV003225631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304709.1:p.Pro148Leu
CA4664058
NM_001317780.2:c.443C>T