Canonical Allele Identifier: PA177971
Gene: SFTPD HGNC NCBI

Linked Data

ClinVar Variation Id: 165219
ClinVar RCV Id: RCV000151865 RCV001689698
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003010.4:p.Met31Thr
CA177970
NM_003019.5:c.92T>C