Canonical Allele Identifier: PA2826970630
Gene: SFTPC HGNC NCBI

Linked Data

ClinVar Variation Id: 13214
ClinVar RCV Id: RCV000014101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304709.1:p.Leu188Pro
CA210546
NM_001317780.2:c.563T>C