Canonical Allele Identifier: PA2827056997
Gene: SFTPA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13199

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307742.1:p.Gly231Val
CA256736
NM_001320813.2:c.692G>T