ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2827056984
Gene: SFTPA2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
985062
ClinVar RCV Id:
RCV001265772
RCV001732099
RCV001780219
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001307742.1:p.Val178Met
CA5574018
NM_001320813.2:c.532G>A