Canonical Allele Identifier: PA2828229844
Gene: SFTPB HGNC NCBI

Linked Data

ClinVar Variation Id: 337301
ClinVar RCV Id: RCV000284887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354210.1:p.Gly310Arg
CA1743859
NM_001367281.1:c.928G>A
CA347487251
NM_001367281.1:c.928G>C