Canonical Allele Identifier: PA1139696915
Gene: SFTPA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 985062
ClinVar RCV Id: RCV001265772 RCV001732099 RCV001780219
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307743.1:p.Val188Met
CA5574018
NM_001320814.1:c.562G>A