Canonical Allele Identifier: PA2826970610
Gene: SFTPC HGNC NCBI

Linked Data

ClinVar Variation Id: 362560
ClinVar RCV Id: RCV000305466 RCV000391181 RCV001358404 RCV002248630
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304709.1:p.Ala149Pro
CA4664059
NM_001317780.2:c.445G>C