Canonical Allele Identifier: PA645490285
Gene: SFTPC HGNC NCBI

Linked Data

ClinVar Variation Id: 362553
ClinVar RCV Id: RCV000306866 RCV000407976
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003009.2:p.Val48Met
CA4663912
NM_003018.4:c.142G>A