Canonical Allele Identifier: PA2825997735
Gene: SFTPA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 165201
ClinVar RCV Id: RCV000151847

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158116.1:p.Pro193Ser
CA177933
NM_001164644.2:c.577C>T