Canonical Allele Identifier: PA2826970396
Gene: SFTPC HGNC NCBI

Linked Data

ClinVar Variation Id: 362554
ClinVar RCV Id: RCV000271807 RCV002248629 RCV000366166 RCV002509375 RCV003556368 RCV002402077
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304707.1:p.His59Arg
CA4663918
NM_001317778.2:c.176A>G