Canonical Allele Identifier: PA2826970613
Gene: SFTPC HGNC NCBI

Linked Data

ClinVar Variation Id: 13209
ClinVar RCV Id: RCV000014096 RCV000261074 RCV002054436 RCV002336082 RCV003904835
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304709.1:p.Arg161Gln
CA210538
NM_001317780.2:c.482G>A