ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA177971
Gene: SFTPD
HGNC
NCBI
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_003010.4:p.Met31Thr
CA177970
NM_003019.5:c.92T>C