Canonical Allele Identifier: PA2580207316
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_001307743.1:p.Ala164Pro
CA5574035
NM_001320814.1:c.490G>C