Canonical Allele Identifier: PA2825997820
Gene: SFTPA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 165201
ClinVar RCV Id: RCV000151847

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158118.1:p.Pro144Ser
CA177933
NM_001164646.2:c.430C>T