ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2827056978
Gene: SFTPA2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1705909
ClinVar RCV Id:
RCV002284283
RCV003883802
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001307742.1:p.Ala154Pro
CA5574035
NM_001320813.2:c.460G>C