Canonical Allele Identifier: PA2828229846
Gene: SFTPB HGNC NCBI

Linked Data

ClinVar Variation Id: 2612913
ClinVar RCV Id: RCV004356291
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354210.1:p.Trp329Ser
CA347486976
NM_001367281.1:c.986G>C