Canonical Allele Identifier: PA2827056996
Gene: SFTPA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1691338
ClinVar RCV Id: RCV002254436
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307742.1:p.Met227Arg
CA377352732
NM_001320813.2:c.680T>G