Canonical Allele Identifier: PA2827056978
Gene: SFTPA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1705909

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307742.1:p.Ala154Pro
CA5574035
NM_001320813.2:c.460G>C