ClinGen Allele Registry
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Canonical Allele Identifier:
PA645490437
Gene: SFTPC
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000305466
RCV000391181
RCV001358404
RCV002248630
ClinVar Variation:
362560
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_003009.2:p.Ala155Pro
CA4664059
NM_003018.4:c.463G>C